Alkyl phenyl sulfide derivative and pest control agent

ABSTRACT

An alkyl phenyl sulfide derivative represented by the general formula [I] or an agriculturally acceptable salt thereof, and a pest control agent containing the derivative or the salt as an active ingredient. 
     
       
         
         
             
             
         
       
     
     [in the above formula, R 1  is, for example, a C 1 ˜C 6  alkyl group which is mono- or poly-substituted with halogen atom; R 2  is, for example, a halogen atom or a C 1 ˜C 6  alkyl group; R 3  is, for example, a hydrogen atom or a halogen atom; and R 4  is, for example, a hydrogen atom or a C 1 ˜C 12  alkyl group.] The derivative or the salt has an excellent pest control effect.

TECHNICAL FIELD

The present invention relates to a novel alkyl phenyl sulfide derivative or an agriculturally acceptable salt thereof, as well as to a pest control agent containing the derivative or the salt thereof as an active ingredient.

BACKGROUND ART

Alkyl phenyl sulfide derivatives having a pest control effect are described in patent literatures 1, 2, 3, 4, 5 and 6. However, the compounds described in the patent literatures 1, 2, 3 and 4 are restricted to alkyl phenyl sulfide derivatives having no substituent group on the alkylthio group; the compounds described in the patent literature 5 are restricted to alkyl phenyl sulfide derivatives having certain substituents on the phenyl ring; and the compounds described in the patent literature 6 are restricted to alkyl phenyl sulfide derivatives having a 2-bromoethylthio group as a substituent group. Thus, these patent literatures make no mention of an alkyl phenyl sulfide derivative having a substituent group other than bromine atom on the alkylthio group.

The follow-up experiment made on the compounds described in the above patent literatures revealed that, despite the description made therein, the compounds have an insufficient effect to spider mites, have no effect to spider mites which have acquired chemical resistance, and accordingly have no sufficient control effect.

Patent literature 1: JP-A-1975-29744

Patent literature 2: JP-A-1976-19121

Patent literature 3: JP-B-1982-35162

Patent literature 4: JP-A-1988-41451

Patent literature 5: JP-A-1992-312566

Patent literature 6: U.S. Pat. No. 3,388,167

SUMMARY OF THE INVENTION

Pest control agent applied to useful crops is desired to be a chemical agent which exhibits a sufficient pest control effect at a low dose when applied to soil or stem and leaf. Also, development of safer pest control agent is desired because requirements for safety of chemical substance and its influence to environment are becoming stronger. Further, in recent years, the use of pest control agents such as insecticide, miticide and the like over many years have invited the appearance of pests which have acquired resistance to such pest control agents, and complete control of pests have become difficult. Furthermore, the use of pest control agents having high toxicity to humans and livestock has become a problem from the safety to workers and others.

Under such circumstances, the task of the present invention is to solve the above-mentioned problems of conventional pest control agents and provide a pest control agent superior in safety, control effect, residual effect, etc.

Means to Solve the Problems

In order to develop a pest control agent having the above-mentioned desirable properties, the present inventors synthesized various alkyl phenyl sulfide derivatives and investigated their physiological activities earnestly. As a result, it was found that an alkyl phenyl sulfide derivative represented by the following general formulas [I] or [I′] (the derivative is hereinafter referred to as the present compound) has an excellent effect on various pests, particularly on spider mites represented by Tetranychus urticae, Tetranychus kanzawai, Panonychus citri, etc. A further research has led to the completion of the present invention.

The present invention is as follows.

(1) An alkyl phenyl sulfide derivative represented by the general formula [I] or an agriculturally acceptable salt thereof

[in the formula [I], n is an integer of 0, 1 or 2, R¹ is a C₁-C₆ haloalkyl group (the group excludes 2-bromoethyl group), a C₂-C₈ alkenyl group (the group excludes allyl group), a C₂-C₈ haloalkenyl group, a C₂-C₆ alkynyl group, a C₂-C₆ haloalkynyl group, a branched C₄-C₆ alkyl group (the group excludes isobutyl group), a C₃-C₆ cycloalkyl C₁-C₆ alkyl group or a C₃-C₆ halocycloalkyl C₁-C₆ alkyl group, R² is a halogen atom, a C₁-C₆ alkyl group, a C₁-C₆ haloalkyl group, a C₃-C₆ cycloalkyl group, a C₃-C₆ halocycloalkyl group, a C₁-C₆ alkoxy group, a C₁-C₆ haloalkoxy group, a cyano group or a nitro group, R³ is a hydrogen atom, a halogen atom, a C₁-C₆ alkyl group or a C₁-C₆ haloalkyl group, R₄ is a C₁-C₁₂ alkyl group (the group may be mono- or poly-substituted with R⁵), a C₃-C₆ cycloalkyl group (the group may be mono- or poly-substituted with R⁵), a C₂-C₈ alkenyl group (the group may be mono- or poly-substituted with R⁵), a C₂-C₆ alkynyl group (the group may be mono- or poly-substituted with R⁵) or a benzoyl group (the group may be mono- or poly-substituted with R⁶), R⁵ is a halogen atom, a C₁-C₆ alkyl group, a C₁-C₆ haloalkyl group, a C₃-C₆ cycloalkyl group (the group may be mono- or poly-substituted with R⁶), a C₃-C₆ halocycloalkyl group, a hydroxyl group, a C₁-C₆ alkoxy group, a C₁-C₆ haloalkoxy group, a C₃-C₆ cycloalkoxy group, a C₃-C₆ halocycloalkoxy group, a C₁-C₆ alkoxy C₁-C₆ alkoxy group, a C₁-C₆ haloalkoxy C₁-C₆ alkoxy group, a C₁-C₆ haloalkoxy C₁-C₆ haloalkoxy group, a C₁-C₆ alkylsulfinyloxy group, a C₁-C₆ haloalkylsulfinyloxy group, a C₃-C₆ cycloalkylsulfinyloxy group, a C₃-C₆ halocycloalkylsulfinyloxy group, a C₁-C₆ alkylsulfonyloxy group, a C₁-C₆ haloalkylsulfonyloxy group, a C₃-C₆ cycloalkylsulfonyloxy group, a C₃-C₆ halocycloalkylsulfonyloxy group, a thiol group, a C₁-C₆ alkylthio group, a C₁-C₆ haloalkylthio group, a C₂-C₆ alkenylthio group, a C₂-C₆ haloalkenylthio group, a C₃-C₆ cycloalkylthio group, a C₃-C₆ halocycloalkylthio group, a C₃-C₆ cycloalkyl C₁-C₆ alkylthio group, a C₃-C₆ halocycloalkyl C₁-C₆ alkylthio group, a tri(C₁-C₆ alkyl)silyl C₁-C₆ alkylthio group, a C₁-C₆ alkylsulfinyl group, a C₁-C₆ haloalkylsulfinyl group, a C₃-C₆ cycloalkylsulfinyl group, a C₃-C₆ halocycloalkylsulfinyl group, a C₁-C₆ alkylsulfonyl group, a C₁-C₆ haloalkylsulfonyl group, a C₃-C₆ cycloalkylsulfonyl group, a C₃-C₆ halocycloalkylsulfonyl group, a C₁-C₆ alkylcarbonyl group, a C₁-C₆ haloalkylcarbonyl group, a formyl group, a C₁-C₆ alkylcarbonyloxy group, a C₁-C₆ haloalkylcarbonyloxy group, a formyloxy group, an amino group, a C₁-C₆ alkylcarbonylamino group (the amino group may be substituted with R⁹), a C₁-C₆ haloalkylcarbonylamino group (the amino group may be substituted with R⁹), a phenylcarbonylamino group (the phenyl group may be mono- or poly-substituted with R⁶, the amino group may be substituted with R⁹), a C₁-C₆ alkoxycarbonylamino group (the amino group may be substituted with R⁹), a C₁-C₆ haloalkoxycarbonylamino group (the amino group may be substituted with R⁹), a C₁-C₆ alkylaminocarbonylamino group (the amino group may be substituted with R⁹), a C₁-C₆ haloalkylaminocarbonylamino group (the amino group may be substituted with R⁹), a C₁-C₆ alkylsulfonylamino group (the amino group may be substituted with R⁹), a C₁-C₆ haloalkylsulfonylamino group (the amino group may be substituted with R⁹), a phenylsulfonylamino group (the phenyl group may be substituted with R⁶, the amino group may be substituted with R⁹), a C₁-C₆ alkylamino group (the amino group may be substituted with R⁹), a C₁-C₆ haloalkylamino group (the amino group may be substituted with R⁹), a C₁-C₆ alkylaminocarbonylthio group (the amino group may be substituted with R⁹), a C₁-C₆ haloalkylaminocarbonylthio group (the amino group may be substituted with R⁹), a C₁-C₆ alkylaminocarbonyl group (the amino group may be substituted with R⁹), a C₁-C₆ haloalkylaminocarbonyl group (the amino group may be substituted with R⁹), a C₁-C₆ alkoxycarbonyl group, a C₁-C₆ haloalkoxycarbonyl group, a tri(C₁-C₆ alkyl)silyl group, a phenyl group (the group may be mono- or poly-substituted with R⁶), a pyridyloxyphenyl group (the pyridyl group may be mono- or poly-substituted with R⁶), a phenoxy group (the group may be mono- or poly-substituted with R⁶), a phenyl C₁-C₆ alkoxy group (the phenyl group may be mono- or poly-substituted with R⁶), a phenylcarbonyloxy group (the phenyl group may be mono- or poly-substituted with R⁶), a phenylcarbonyl group (the phenyl group may be mono- or poly-substituted with R⁶), a benzoyl group (the group may be mono- or poly-substituted with R⁶), a benzoyloxy group (the group may be mono- or poly-substituted with R⁶), a phenylthio group (the group may be mono- or poly-substituted with R⁶), a phenylsulfonyl group (the group may be mono- or poly-substituted with R⁶), a phenylsulfinyl group (the group may be mono- or poly-substituted with R⁶), a phenyl C₁-C₆ alkylthio group (the phenyl group may be mono- or poly-substituted with R⁶), a phenyl C₁-C₆ alkylsulfinyl group (the phenyl group may be mono- or poly-substituted with R⁶), a phenyl C₁-C₆ alkylsulfonyl group (the phenyl group may be mono- or poly-substituted with R⁶), a —O—N═C(R⁷)(R⁸) group, an adamantyl group, a pyrrolyl group (the group may be mono- or poly-substituted with R⁶), a pyrazolyl group (the group may be mono- or poly-substituted with R⁶), an imidazolyl group (the group may be mono- or poly-substituted with R⁶), a triazolyl group (the group may be mono- or poly-substituted with R⁶), an oxazolyl group (the group may be mono- or poly-substituted with R⁶), an isoxazolyl group (the group may be mono- or poly-substituted with R⁶), a thiazolyl group (the group may be mono- or poly-substituted with R⁶), an isothiazolyl group (the group may be mono- or poly-substituted with R⁶), a pyridyl group (the group may be mono- or poly-substituted with R⁶ and the nitrogen atom of the group may be oxidized to form N-oxide), a pyrimidinyl group (the group may be mono- or poly-substituted with R⁶), a pyridyloxy group (the group may be mono- or poly-substituted with R⁶), a tetrahydrofuranyl group (the group may be mono- or poly-substituted with R⁶), 1,3-dioxoisoindolinyl group (the group may be mono- or poly-substituted with R⁶), a cyano group, a nitro group, a carboxyl group, a thiocyanato group or an aminoxy group, R⁶ is a halogen atom, a C₁-C₆ alkyl group, a C₁-C₆ haloalkyl group, a C₃-C₆ cycloalkyl group, a C₃-C₆ halocycloalkyl group, a C₃-C₆ cycloalkyl C₁-C₆ alkyl group, a C₃-C₆ halocycloalkyl C₁-C₆ alkyl group, a C₁-C₆ alkoxy group, a C₁-C₆ haloalkoxy group, a C₁-C₆ alkylthio group, a C₁-C₆ haloalkylthio group, a C₁-C₆ alkylsulfinyl group, a C₁-C₆ haloalkylsulfinyl group, a C₁-C₆ alkylsulfonyl group, a C₁-C₆ haloalkylsulfonyl group, a C₁-C₆ alkylthio C₁-C₆ alkyl group, a C₁-C₆ haloalkylthio C₁-C₆ alkyl group, a C₁-C₆ alkylsulfonyloxy group, a C₁-C₆ haloalkylsulfonyloxy group, a phenyl group (the group may be mono- or poly-substituted with halogen atom, alkyl group or haloalkyl group), a phenyl C₁-C₆ alkyl group, a phenyl C₁-C₆ alkoxy group, a cyano group or a nitro group, R⁷ and R⁸ may be the same or different, are each a hydrogen atom, a C₁-C₆ alkyl group, a C₁-C₆ haloalkyl group, a C₃-C₆ cycloalkyl group, a C₃-C₆ halocycloalkyl group or a phenyl group (the group may be mono- or poly-substituted with R⁶), and may form a 3- to 6-membered ring together with the carbon atom to which they bond, and R⁹ is a C₁-C₆ alkyl group, a C₁-C₆ haloalkyl group, a C₃-C₆ cycloalkyl group, a C₃-C₆ halocycloalkyl group, a C₁-C₆ alkylcarbonyl group, a C₁-C₆ haloalkylcarbonyl group, a C₁-C₆ alkoxycarbonyl group, a C₁-C₆ haloalkoxycarbonyl group, a C₁-C₆ alkylaminocarbonyl group, a C₁-C₆ haloalkylaminocarbonyl group or benzoyl group (the group may be mono- or poly-substituted with R⁶]. (2) An alkyl phenyl sulfide derivative or an agriculturally acceptable salt thereof, set forth in (1), wherein R¹ in the general formula [I] is a 2,2-difluoroethyl group, a 2,2,2-trifluoroethyl group, a 3,3,3-trifluoropropyl group, a pentafluoroethyl group, 1,2,2,2-tetrafluoroethyl group, 2-chloro-2,2-difluoroethyl group, a 2,2,3,3-tetrafluoropropyl group, a 2,2,3,3,3-pentafluoropropyl group, a 3,3-dichloroallyl group, a propargyl group, a cyclopropylmethyl group or a (2,2-difluorocyclopropyl)methyl group. (3) An alkyl phenyl sulfide derivative or an agriculturally acceptable salt thereof, set forth in (1) or (2), wherein R² in the general formula [I] is a halogen atom, a C₁-C₆ alkyl group, a C₁-C₆ haloalkyl group or a cyano group. (4) An alkyl phenyl sulfide derivative or an agriculturally acceptable salt thereof, set forth in any of (1) to (3), wherein R³ in the general formula [I] is a hydrogen atom, a halogen atom or a C₁-C₆ alkyl group. (5) A pest control agent which contains, as an active ingredient, an alkyl phenyl sulfide derivative or an agriculturally acceptable salt thereof, set forth in any of (1) to (4). (6) An alkyl phenyl sulfide derivative represented by the general formula [I′] or a salt thereof

wherein n is an integer of 0, 1 or 2, R^(1′) is a C₁-C₆ haloalkyl group (the group excludes 2-bromoethyl group), a C₂-C₈ alkenyl group (the group excludes allyl group), a C₂-C₈ haloalkenyl group, a C₂-C₆ alkynyl group, a C₂-C₆ haloalkynyl group, a branched C₄-C₆ alkyl group (the group excludes isobutyl group), a C₃-C₆ cycloalkyl C₁-C₆ alkyl group or a C₃-C₆ halocycloalkyl C₁-C₆ alkyl group, R^(2′) is a halogen atom, a C₁-C₆ alkyl group, a C₁-C₆ haloalkyl group, a C₃-C₆ cycloalkyl group, a C₃-C₆ halocycloalkyl group, a C₁-C₆ alkoxy group, a C₁-C₆ haloalkoxy group, a cyano group or a nitro group, R^(3′) is a hydrogen atom, a halogen atom, a C₁-C₆ alkyl group or a C₁-C₆ haloalkyl group.] (7) An alkyl phenyl sulfide derivative or an agriculturally acceptable salt thereof, set forth in (6), wherein R^(1′) in the general formula [I′] is a 2,2-difluoroethyl group, a 2,2,2-trifluoroethyl group, a 3,3,3-trifluoropropyl group, a pentafluoroethyl group, a 1,2,2,2-tetrafluoroethyl group, a 2-chloro-2,2-difluoroethyl group, a 2,2,3,3-tetrafluoropropyl group a 2,2,3,3,3-pentafluoropropyl group, a 3,3-dichloroallyl group, a propargyl group, a cyclopropylmethyl group or a (2,2-difluorocyclopropyl)methyl group. (8) An alkyl phenyl sulfide derivative represented by the general formula [I′] or an agriculturally acceptable salt thereof, set forth in (6) or (7), wherein R^(2′) in the general formula [I′] is a halogen atom, a C₁-C₆ alkyl group, a C₁-C₆ haloalkyl group or a cyano group. (9) An alkyl phenyl sulfide derivative represented by the general formula [I′] or an agriculturally acceptable salt thereof, set forth in any of (6) to (8), wherein R^(3′) in the general formula [I′] is a hydrogen atom, a halogen atom or a C₁-C₆ alkyl group.

Advantages of the Invention

The pest control agent containing the present compound has an excellent effect to a wide range of pests such as Hemiptera, Lepidoptera, Coleoptera, Diptera, Hymenoptera, Orthoptera, Order Isoptera, Thysanoptera, spider mites, plant parasitic nematodes and the like and can control even pests which have acquired chemical resistance.

In particular, the pest control agent containing the present compound has an excellent effect to spider mites as pest, represented by Tetranychus urticae, Tetranychus kanzawai, Panonychus citri, etc., and has a sufficient effect even to spider mites which have acquired chemical resistance.

The symbols and terms used in this Specification are explained.

In the present invention, pest control agent means insecticide, miticide, nematicide, etc., used in agricultural and horticultural field, animals (e.g. livestock and pets), household, or infectious disease control.

In the present invention, halogen atom indicates fluorine atom, chlorine atom, bromine atom or iodine atom.

In the present invention, expression such as C₁-C₆ indicates that the substituent group after the expression has 1 to 6 carbon atoms in this case.

In the present invention, C₁-C₆ alkyl group indicates a straight chain or branched chain alkyl group having 1 to 6 carbon atoms, unless otherwise specified. There can be mentioned, for example, groups such as methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert-butyl, n-pentyl, 1-methylbutyl, 2-methylbutyl, 3-methylbutyl, 1-ethylpropyl, 1,1-dimethylpropyl, 1,2-dimethylpropyl, neopentyl, n-hexyl, 1-methylpentyl, 2-methylpentyl, 3-methylpentyl, 4-methylpentyl, 1-ethylbutyl, 2-ethylbutyl, 1,1-dimethylbutyl, 1,2-dimethylbutyl, 1,3-dimethylbutyl, 2,2-dimethylbutyl, 2,3-dimethylbutyl, 3,3-dimethylbutyl, 1,1,2-trimethylpropyl, 1,2,2-trimethylpropyl, 1-ethyl-1-methylpropyl and 1-ethyl-2-methylpropyl.

In the present invention, C₁-C₆ haloalkyl group indicates a straight chain or branched chain haloalkyl group having 1 to 6 carbon atoms, substituted with 1 to 13 same or different halogen atoms, unless otherwise specified. There can be mentioned, for example, fluoromethyl, difluoromethyl, trifluoromethyl, chloromethyl, dichloromethyl, trichloromethyl, bromomethyl, dibromomethyl, tribromomethyl, iodomethyl, chlorodifluoromethyl, dichlorofluoromethyl, 1-fluoroethyl, 2-fluoroethyl, 1,1-difluoroethyl, 2,2-difluoroethyl, 2,2,2-trifluoroethyl, 1,1,2,2-tetrafluoroethyl, pentafluoroethyl, 1-chloroethyl, 2-chloroethyl, 1,1-dichloroethyl, 2,2-dichloroethyl, 2,2,2-trichloroethyl, 1,1,2,2-tetrachloroethyl, pentachloroethyl, 1-bromoethyl, 2-bromoethyl, 2,2,2-tribromoethyl, 1-iodoethyl, 2-iodoethyl, 2-chloro-2,2-difluoroethyl, 2,2-dichloro-2-fluoroethyl, 2-trichloroethyl, 1-fluoropropyl, 2-fluoropropyl, 3-fluoropropyl, 1,1-difluoropropyl, 2,2-difluoropropyl, 3,3-difluoropropyl, 3,3,3-trifluoropropyl, 2,2,3,3,3-pentafluoropropyl, heptafluoropropyl, 1-fluoropropane-2-yl, 2-fluoropropane-2-yl, 1,1-difluoropropane-2-yl, 1,2-difluoropropane-2-yl, 1,3-difluoropropane-2-yl, 1,2,3-trifluoropropane-2-yl, 1,1,3,3-tetrafluoropropane-2-yl, 1,1,1,3,3,3-hexafluoropropane-2-yl, heptafluoropropane-2-yl, 1-chloropropyl, 2-chloropropyl, 3-chloropropyl, 1,1-dichloropropyl, 2,2-dichloropropyl, 3,3-dichloropropyl, 3,3,3-trichloropropyl, 2,2,3,3,3-pentachloropropyl, heptachloropropyl, 1-chloropropane-2-yl, 2-chloropropane-2-yl, 1,1-dichloropropane-2-yl, 1,2-dichloropropane-2-yl, 1,3-dichloropropane-2-yl, 1,2,3-trichloropropane-2-yl, 1,1,3,3-tetrachloropropane-2-yl, 1,1,1,3,3,3-hexachloropropane-2-yl, heptachloropropane-2-yl, 1-bromopropyl, 2-bromopropyl, 3-bromopropyl, 1-bromopropane-2-yl, 2-bromopropane-2-yl, 1-iodopropyl, 2-iodopropyl, 3-iodopropyl, 1-iodopropane-2-yl, 2-iodopropane-2-yl, 1-fluorobutyl, 2-fluorobutyl, 3-fluorobutyl, 4-fluorobutyl, 4,4-difluorobutyl, 4,4,4-trifluorobutyl, 3,3,4,4,4-pentafluorobutyl, 2,2,3,3,4,4,4-heptafluorobutyl, nonafluorobutyl, 1,1,1-trifluorobutane-2-yl 4,4,4-trifluorobutane-2-yl, 3,3,4,4,4-pentafluorobutane-2-yl, nonafluorobutane-2-yl, 1,1,1,3,3,3-hexafluoro-2-(trifluoromethyl)propane-2-yl, 1-chlorobutyl, 2-chlorobutyl, 3-chlorobutyl, 4-chlorobutyl, 4,4-dichlorobutyl, 4,4,4-trichlorobutyl, nonachlorobutyl, 1,1,1-trichlorobutane-2-yl 4,4,4-trichlorobutane-2-yl, nonachlorobutane-2-yl, 1-bromobutyl, 2-bromobutyl, 3-bromobutyl, 4-bromobutyl, 1-iodobutyl, 2-iodobutyl, 3-iodobutyl, 4-iodobutyl, 4-chloro-1,1,2,2,3,3,4,4-octafluorobutyl, 4-bromo-1,1,2,2,3,3,4,4-octafluorobutyl, 1-fluoropentyl, 2-fluoropentyl, 3-fluoropentyl, 4-fluoropentyl, 5-fluoropentyl, 5,5,5-trifluoropentyl, 4,4,5,5,5-pentafluoropentyl, 3,3,4,4,5,5,5-heptafluoropentyl, 2,2,3,3,4,4,5,5,5-nonafluoropentyl, undecafluoropentyl, 1-chloropentyl, 2-chloropentyl, 3-chloropentyl, 4-chloropentyl, 5-chloropentyl, 5,5,5-trichloropentyl, 4,4,5,5,5-pentachloropentyl, 3,3,4,4,5,5,5-heptachloropentyl, 2,2,3,3,4,4,5,5,5-nonachloropentyl, undecachloropentyl, 1-bromopentyl, 2-bromopentyl, 3-bromopentyl, 4-bromopentyl, 5-bromopentyl, 5-iodopentyl, 1-fluorohexyl, 2-fluorohexyl, 3-fluorohexyl, 4-fluorohexyl, 5-fluorohexyl, 6-fluorohexyl, 6,6,6-trifluorohexyl, 5,5,6,6,6-pentafluorohexyl, 4,4,5,5,6,6,6-heptafluorohexyl, 3,3,4,4,5,5,6,6,6-nonafluorohexyl, 2,2,3,3,4,4,5,5,6,6,6-undecafluorohexyl, tridecafluorohexyl, 1-chlorohexyl, 2-chlorohexyl, 3-chlorohexyl, 4-chlorohexyl, 5-chlorohexyl, 6-chlorohexyl, 5-bromohexyl, 6-bromohexyl, 5-iodohexyl and 6-iodohexyl.

In the present invention, C₁-C₁₂ alkyl group indicates a straight chain or branched chain alkyl group having 1 to 12 carbon atoms, unless otherwise specified. There can be mentioned, in addition to the above-mentioned C₁-C₆ carbon atoms, for example, n-heptyl, n-octyl, n-nonyl, n-decyl, n-undecyl, n-dodecyl, 4,4-dimethylpentyl, 5-methylhexyl, 5,5-dimethylhexyl, 3,5,5-trimethylhexyl, 6-methylheptyl, 6,6-dimethylheptyl, 3,6,6-trimethylheptyl, 7-methyloctyl, 7,7-dimethyloctyl, 8-methylnonyl, 8,8-dimethylnonyl, 9-methyldecyl, 9,9-dimethyldecyl and 10-methylundecyl.

In the present invention, branched chain C₄-C₆ alkyl group indicates a branched chain alkyl group having 4 to 6 carbon atoms, unless otherwise specified. There can be mentioned, for example, groups such as sec-butyl, isobutyl, tert-butyl, 1-methylbutyl, 2-methylbutyl, 3-methylbutyl, 1-ethylpropyl, 1,1-dimethylpropyl, 1,2-dimethylpropyl, neopentyl, 1-methylpentyl, 2-methylpentyl, 3-methylpentyl, 4-methylpentyl, 1-ethylbutyl, 2-ethylbutyl, 1,1-dimethylbutyl, 1,2-dimethylbutyl, 1,3-dimethylbutyl, 2,2-dimethylbutyl, 2,3-dimethylbutyl, 3,3-dimethylbutyl, 1,1,2-trimethylpropyl, 1,2,2-trimethylpropyl, 1-ethyl-1-methylpropyl and 1-ethyl-2-methylpropyl.

In the present invention, C₃-C₆ cycloalkyl group indicates a cycloalkyl group having 3 to 6 carbon atoms, unless otherwise specified. There can be mentioned, for example, groups such as cyclopropyl, cyclobutyl, cyclopentyl and cyclohexyl.

In the present invention, C₃-C₆ halocycloalkyl group indicates a cycloalkyl group having 3 to 6 carbon atoms, substituted with 1 to 11 same or different halogen atoms, unless otherwise specified. There can be mentioned, for example, groups such as 1-fluorocyclopropyl, 2-fluorocyclopropyl, 2,2-difluorocyclopropyl, 2,2,3,3-tetrafluorocyclopropyl, 1-chlorocyclopropyl, 2-chlorocyclopropyl, 2,2-dichlorocyclopropyl, 2,2,3,3-tetrachlorocyclopropyl, 2,2-dibromocyclopropyl, 2,2-diiodocyclopropyl, 1-fluorocyclobutyl, 2-fluorocyclobutyl, 3-fluorocyclobutyl, 3,3-difluorocyclobutyl, heptafluorocyclobutyl, 2-chlorocyclobutyl, 3-chlorocyclobutyl, 3,3-dichlorocyclobutyl, 3,3-dibromocyclobutyl, 3,3-diiodocyclobutyl, 1-fluorocyclopentyl, 2-fluorocyclopentyl, 3-fluorocyclopentyl, 2,2-difluorocyclopentyl, 3,3-difluorocyclopentyl, nonafluorocyclopentyl, 2,2-dichlorocyclopentyl, 3,3-dichlorocyclopentyl, 2,2-dibromocyclopentyl, 3,3-dibromocyclopentyl, 2,2-diiodocyclopentyl, 3,3-diiodocyclopentyl, 1-fluorocyclohexyl, 2-fluorocyclohexyl, 3-fluorocyclohexyl, 4-fluorocyclohexyl, 2,2-difluorocyclohexyl, 3,3-difluorocyclohexyl, 4,4-difluorocyclohexyl, 1-chlorocyclohexyl, 2-chlorocyclohexyl, 3-chlorocyclohexyl, 4-chlorocyclohexyl, 2,2-dichlorocyclohexyl, 3,3-dichlorocyclohexyl, 4,4-dichlorocyclohexyl, 3,3-dibromocyclohexyl, 4,4-dibromocyclohexyl, 3,3-diiodocyclohexyl and 4,4-diiodocyclohexyl.

In the present invention, C₂-C₈ alkenyl group indicates a straight chain or branched chain alkenyl group having 2 to 8 carbon atoms, unless otherwise specified. There can be mentioned, for example, groups such as vinyl, 1-propenyl, isopropenyl, 2-propenyl, 1-butenyl, 1-methyl-1-propenyl, 2-butenyl, 1-methyl-2-propenyl, 3-butenyl, 2-methyl-1-propenyl, 2-methyl-2-propenyl, 1,3-butadienyl, 1-pentenyl, 1-ethyl-2-propenyl, 2-pentenyl, 1-methyl-1-butenyl, 3-pentenyl, 1-methyl-2-butenyl, 4-pentenyl, 1-methyl-3-butenyl, 3-methyl-1-butenyl, 1,2-dimethyl-2-propenyl, 1,1-dimethyl-2-propenyl, 2-methyl-2-butenyl, 3-methyl-2-butenyl, 1,2-dimethyl-1-propenyl, 2-methyl-3-butenyl, 3-methyl-3-butenyl, 1,3-pentadienyl, 2,3-butadien-1-yl, 1-vinyl-2-propenyl, 1-hexenyl, 1-propyl-2-propenyl, 2-hexenyl, 1-methyl-1-pentenyl, 1-ethyl-2-butenyl, 3-hexenyl, 4-hexenyl, 5-hexenyl, 1-methyl-4-pentenyl, 1-ethyl-3-butenyl, 1-(isobutyl)vinyl, 1-ethyl-1-methyl-2-propenyl, 1-ethyl-2-methyl-2-propenyl, 1-(isopropyl)-2-propenyl, 2-methyl-2-pentenyl, 3-methyl-3-pentenyl, 4-methyl-3-pentenyl, 1,3-dimethyl-2-butenyl, 1,1-dimethyl-3-butenyl, 3-methyl-4-pentenyl, 4-methyl-4-pentenyl, 1,2-dimethyl-3-butenyl, 1,3-dimethyl-3-butenyl, 1,1,2-trimethyl-2-propenyl, 1,5-hexadienyl, 1-vinyl-3-butenyl, 2,4-hexadienyl, 2-octenyl and 3,7-dimethyl-6-octenyl.

In the present invention, C₂-C₈ haloalkenyl group indicates a haloalkenyl group having 2 to 8 carbon atoms, substituted with 1 to 15 same or different halogen atoms, unless otherwise specified. There can be mentioned, for example, groups such as 1-fluorovinyl, 2-fluorovinyl, 1,2-difluorovinyl, 2,2-difluorovinyl, trifluorovinyl, 1-chlorovinyl, 2-chlorovinyl, dichlorovinyl, trichlorovinyl, dibromovinyl, diiodovinyl, 1-fluoro-2-propenyl, 2-fluoro-2-propenyl, 3-fluoro-2-propenyl, 2,3-difluoro-2-propenyl, 3,3-difluoro-2-propenyl, 3,3-difluoro-1-propenyl, 2,3,3-trifluoro-2-propenyl, 3,3,3-trifluoro-1-propenyl, 1,2,3,3,3-pentafluoro-1-propenyl, 1-chloro-2-propenyl, 2-chloro-2-propenyl, 3-chloro-2-propenyl, 2,3-dichloro-2-propenyl, 3,3-dichloro-2-propenyl, 3,3-dichloro-1-propenyl, 2,3,3-trichloro-2-propenyl, 3,3,3-trichloro-1-propenyl, 3-bromo-2-propenyl, 3,3-dibromo-2-propenyl, 3,3-diiodo-2-propenyl, 2,2-difluoro-1-propen-2-yl, 3,3,3-trifluoro-1-propen-2-yl, 3,3,3-trichloro-1-propen-2-yl, 4-fluoro-3-butenyl, 4,4-difluoro-3-butenyl, 4,4-difluoro-3-buten-2-yl, 4,4,4-trifluoro-2-butenyl, 3,4,4-trifluoro-3-butenyl, 2-trifluoromethyl-2-propenyl, 2-trifluoromethyl-3,3-difluoro-2-propenyl, 4,4,4-trifluoro-3-chloro-2-butenyl, 4,4-dichloro-3-butenyl, 4,4,4-trichloro-2-butenyl, 2-trichloromethyl-2-propenyl, 5,5-difluoro-4-pentenyl, 4,5,5-trifluoro-4-pentenyl, 5,5,5-trifluoro-3-pentenyl, 4,4,4-trifluoro-3-methyl-2-butenyl, 4,4,4-trifluoro-3-trifluoromethyl-2-butenyl, 5,5-dichloro-4-pentenyl, 4,4,4-trichloro-3-methyl-2-butenyl, 6,6-difluoro-5-hexenyl, 5,6,6-trifluoro-5-pentenyl, 6,6,6-trifluoro-4-pentenyl, 5,5,5-trifluoro-4-methyl-3-pentenyl, 5,5,5-trifluoro-4-trifluoromethyl-3-pentenyl, 6,6-dichloro-5-hexenyl and 5,5,5-trichloro-4-methyl-3-pentenyl.

In the present invention, C₂-C₆ alkynyl group indicates a straight chain or branched chain alkynyl group having 2 to 6 carbon atoms, unless otherwise specified. There can be mentioned, for example, groups such as ethynyl, 1-propynyl, 2-propynyl, 1-butynyl, 1-methyl-2-propynyl, 2-butynyl, 3-butynyl, 1-pentynyl, 1-ethyl-2-propynyl, 2-pentynyl, 3-pentynyl, 1-methyl-2-butynyl, 4-pentynyl, 1-methyl-3-butynyl, 2-methyl-3-butynyl, 1-hexynyl, 1-(n-propyl)-2-propynyl, 2-hexynyl, 1-ethyl-2-butynyl, 3-hexynyl, 1-methyl-2-pentynyl, 1-methyl-3-pentynyl, 4-methyl-1-pentynyl, 3-methyl-1-pentynyl, 5-hexynyl, 1-ethyl-3-butynyl, 1-ethyl-1-methyl-2-propynyl, 1-(isopropyl)-2-propynyl, 1,1-dimethyl-2-butynyl and 2,2-dimethyl-3-butynyl.

In the present invention, C₂-C₆ haloalkynyl group indicates a straight chain or branched chain haloalkynyl group having 2 to 6 carbon atoms, substituted with 1 to 9 same or different halogen atoms, unless otherwise specified. There can be mentioned, for example, groups such as fluoroethynyl, chloroethynyl, bromoethynyl, iodoethynyl, 3-fluoro-2-propynyl, 3-chloro-2-propynyl, 3-bromo-2-propynyl, 3-iodo-2-propynyl, 4-fluoro-3-butynyl, 4-chloro-3-butynyl, 4-bromo-3-butynyl, 4-iodo-3-butynyl, 4,4-difluoro-2-butynyl, 4,4-dichloro-2-butynyl, 4,4,4-trifluoro-2-butynyl, 4,4,4-trichloro-2-butynyl, 3-fluoro-1-methyl-2-propynyl, 3-chloro-1-methyl-2-propynyl, 5-fluoro-4-pentynyl, 5-chloro-4-pentynyl, 5,5,5-trifluoro-3-pentynyl, 5,5,5-trichloro-3-pentynyl, 4-fluoro-2-methyl-3-butynyl, 4-chloro-2-methyl-3-butynyl, 6-fluoro-5-hexynyl, 6-chloro-5-hexynyl, 6,6,6-trifluoro-4-hexynyl, 6,6,6-trichloro-4-hexynyl, 5-fluoro-3-methyl-4-pentynyl and 5-chloro-3-methyl-4-pentynyl.

In the present invention, C₃-C₆ cycloalkyl C₁-C₆ alkyl group indicates a (C₃-C₆ cycloalkyl)-(C₁-C₆ alkyl) group wherein the cycloalkyl and alkyl has the above-mentioned meaning, unless otherwise specified. There can be mentioned, for example, groups such as cyclopropylmethyl, 2-cyclopropylethyl, 3-cyclopropylpropyl, 4-cyclopropylbutyl, 5-cyclopropylpentyl, 6-cyclopropylhexyl, cyclobutylmethyl, cyclopentylmethyl and cyclohexylmethyl.

In the present invention, C₃-C₆ halocycloalkyl C₁-C₆ alkyl group indicates a (C₃-C₆ halocycloalkyl)-(C₁-C₆ alkyl) group wherein the halocycloalkyl and alkyl has the above-mentioned meaning, unless otherwise specified. There can be mentioned, for example, groups such as 1-fluorocyclopropylmethyl, 2-fluorocyclopropylmethyl, 2,2-difluorocyclopropylmethyl, 2-chlorocyclopropylmethyl, 2,2-dichlorocyclopropylmethyl, 2,2-dibromocyclopropylmethyl, 2,2-diiodorocyclopropylmethyl, 2-(2,2-difluorocyclopropyl)ethyl, 2-(2,2-dichlorocyclopropyl)ethyl, 3-(2,2-difluorocyclopropyl)propyl, 4-(2,2-difluorocyclopropyl)butyl, 5-(2,2-dichlorocyclopropyl)pentyl, 5-(2,2-difluorocyclopropyl)pentyl, 6-(2,2-difluorocyclopropyl)hexyl, 2,2-difluorocyclobutylmethyl, 2,2-dichlorocyclobutylmethyl, 3,3-difluorocyclopentylmethyl, 3,3-dichlorocyclopentylmethyl, 4,4-difluorocyclohexylmethyl and 4,4-dichlorocyclohexylmethyl.

In the present invention, C₁-C₆ alkoxy group indicates a (C₁-C₆ alkyl)-O— group wherein the alkyl has the above-mentioned meaning, unless otherwise specified. There can be mentioned, for example, groups such as methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy, isobutoxy, sec-butoxy, tert-butoxy, n-pentoxy, 1-methylbutoxy, 2-methylbutoxy, 3-methylbutoxy, 1-ethylpropoxy, 1,1-dimethylpropoxy, 1,2-dimethylpropoxy and n-hexyloxy.

In the present invention, C₁-C₆ haloalkoxy group indicates a (C₁-C₆ haloalkyl)-O— group wherein the haloalkyl has the above-mentioned meaning, unless otherwise specified. There can be mentioned, for example, groups such as difluoromethoxy, trifluoromethoxy, trichloromethoxy, tribromomethoxy, 2,2,2-trifluoroethoxy, 2,2,2-trichloroethoxy, pentafluoroethoxy, 3,3,3-trifluoropropoxy, heptafluoro-2-propoxy, tri(trifluoromethyl)methoxy, 3,3,3-trichloropropoxy and heptafluoropropoxy.

In the present invention, C₃-C₆ cycloalkoxy group indicates a (C₃-C₆ cycloalkyl)-O— group wherein the cycloalkyl has the above-mentioned meaning, unless otherwise specified. There can be mentioned, for example, groups such as cyclopropoxy, cyclobutoxy, cyclopentyloxy and cyclohexyloxy.

In the present invention, C₃-C₆ halocycloalkoxy group indicates a (C₃-C₆ halocycloalkyl)-O— group wherein the halocycloalkyl has the above-mentioned meaning, unless otherwise specified. There can be mentioned, for example, groups such as 2,2-difluorocyclopropoxy, 2,2-dichlorocyclopropoxy, 3,3-difluorocyclobutoxy, 3,3-dichlorocyclobutoxy, 3-fluorocyclopentyloxy, 3,3-difluorocyclopentyloxy, nonafluorocyclopentyloxy, 3,3-dichlorocyclopentyloxy, 4,4-difluorocyclohexyloxy, and 4,4-dichlorocyclohexyloxy.

In the present invention, C₁-C₆ alkoxy C₁-C₆ alkoxy group indicates a (C₁-C₆ alkoxy)-(C₁-C₆ alkoxy)- group wherein the alkoxy has the above-mentioned meaning, unless otherwise specified. There can be mentioned, for example, groups such as 2-methoxyethoxy, 3-methoxypropoxy, 2-ethoxyisopropoxy, 2-isopropoxybutoxy, 5-ethoxypentyloxy, 6-ethoxyhexyloxy, 2-(tert-butoxy)ethoxy, 2-methoxyisopentyloxy and 2-isopropoxyisobutoxy.

In the present invention, C₁-C₆ haloalkoxy C₁-C₆ alkoxy group indicates a (C₁-C₆ haloalkoxy)-(C₁-C₆ alkoxy)- group wherein the haloalkoxy and alkoxy has the above-mentioned meaning, unless otherwise specified. There can be mentioned, for example, groups such as 2-difluoromethoxyethoxy, 2-trifluoromethoxyethoxy, 3-trifluoromethoxypropoxy and 2-(2,2,2-trifluoroethoxy)ethoxy.

In the present invention, C₁-C₆ haloalkoxy C₁-C₆ haloalkoxy group indicates a (C₁-C₆ haloalkoxy)-(C₁-C₆ haloalkoxy)- group wherein the haloalkoxy has the above-mentioned meaning, unless otherwise specified. There can be mentioned, for example, groups such as 2-(difluoromethoxy)-1,1,2,2-tetrafluoroethoxy, 2-(trifluoromethoxy)-1,1,2,2-tetrafluoroethoxy, 1,1,2,3,3,3-hexafluoro-2-(hexafluoropropoxy)propoxy, and 2-(2,2,2-trifluoroethoxy)-1,1,2,2-tetrafluoroethoxy.

In the present invention, C₁-C₆ alkylsulfinyloxy group indicates a (C₁-C₆ alkyl)-SO—O— group wherein the alkyl has the above-mentioned meaning, unless otherwise specified. There can be mentioned, for example, groups such as methylsulfinyloxy, ethylsulfinyloxy, n-propylsulfinyloxy and isopropylsulfinyloxy.

In the present invention, C₁-C₆ haloalkylsulfinyloxy group indicates a (C₁-C₆ haloalkyl)-SO—O— group wherein the haloalkyl has the above-mentioned meaning, unless otherwise specified. There can be mentioned, for example, groups such as difluoromethylsulfinyloxy, trifluoromethylsulfinyloxy, 2,2,2-trifluoroethylsulfinyloxy, pentafluoroethylsulfinyloxy, heptafluoropropylsulfinyloxy, trichloromethylsulfinyloxy and heptafluoro-2-propylsulfinyloxy.

In the present invention, C₃-C₆ cycloalkylsulfinyloxy group indicates a (C₃-C₆ cycloalkyl)-SO—O— group wherein the cycloalkyl has the above-mentioned meaning, unless otherwise specified. There can be mentioned, for example, groups such as cyclopropylsulfinyloxy, cyclobutylsulfinyloxy, cyclopentylsulfinyloxy and cyclohexylsulfinyloxy.

In the present invention, C₃-C₆ halocycloalkylsulfinyloxy group indicates a (C₃-C₆ halocycloalkyl)-SO—O— group wherein the halocycloalkyl has the above-mentioned meaning, unless otherwise specified. There can be mentioned, for example, groups such as 2,2-difluorocyclopropylsulfinyloxy, 2,2-dichlorocyclopropylsulfinyloxy, 3,3-difluorocyclobutylsulfinyloxy, 3,3-difluorocyclopentylsulfinyloxy and 4,4-difluorocyclohexylsulfinyloxy.

In the present invention, C₁-C₆ alkylsulfonyloxy group indicates a (C₁-C₆ alkyl)-SO₂—O— group wherein the alkyl has the above-mentioned meaning, unless otherwise specified. There can be mentioned, for example, groups such as methylsulfonyloxy, ethylsulfonyloxy, n-propylsulfonyloxy and isopropylsulfonyloxy.

In the present invention, C₁-C₆ haloalkylsulfonyloxy group indicates a (C₁-C₆ haloalkyl)-SO₂—O— group wherein the haloalkyl has the above-mentioned meaning, unless otherwise specified. There can be mentioned, for example, groups such as difluoromethylsulfonyloxy, trifluoromethylsulfonyloxy, trichloromethylsulfonyloxy, 2,2,2-trifluoroethylsulfonyloxy, 2,2,2-trichloroethylsulfonyloxy, 3,3,3-trifluoropropylsulfonyloxy, heptafluoro-2-propylsulfonyloxy and perfluorobutylsulfonyloxy.

In the present invention, C₃-C₆ cycloalkylsulfonyloxy group indicates a (C₃-C₆ cycloalkyl)-SO₂—O— group wherein the cycloalkyl has the above-mentioned meaning, unless otherwise specified. There can be mentioned, for example, groups such as cyclopropylsulfonyloxy, cyclobutylsulfonyloxy, cyclopentylsulfonyloxy and cyclohexylsulfonyloxy.

In the present invention, C₃-C₆ halocycloalkylsulfonyloxy group indicates a (C₃-C₆ halocycloalkyl)-SO₂—O— group wherein the halocycloalkyl has the above-mentioned meaning, unless otherwise specified. There can be mentioned, for example, groups such as 2,2-difluorocyclopropylsulfonyloxy, 2,2-dichlorocyclopropylsulfonyloxy, 3,3-difluorocyclobutylsulfonyloxy, 3,3-cyclopentylsulfonyloxy and 4,4-difluorocyclohexylsulfonyloxy.

In the present invention, C₁-C₆ alkylthio group indicates a (C₁-C₆ alkyl)-S— group wherein the alkyl has the above-mentioned meaning, unless otherwise specified. There can be mentioned, for example, groups such as methylthio, ethylthio, n-propylthio, isopropylthio, n-butylthio, isobutylthio, sec-butylthio, tert-butylthio and neo-pentylthio.

In the present invention, C₁-C₆ haloalkylthio group indicates a (C₁-C₆ haloalkyl)-S— group wherein the haloalkyl has the above-mentioned meaning, unless otherwise specified. There can be mentioned, for example, groups such as fluoromethylthio, difluoromethylthio, trifluoromethylthio, trichloromethylthio, 2,2,2-trifluoroethylthio, pentafluoroethylthio, 2,2,2-trichloroethylthio, 3,3,3-trifluoropropylthio, heptafluoropropylthio, 1,1,1,3,3,3-hexafluoropropane-2-yl-thio, heptafluoropropane-2-yl-thio, 4,4,4-trifluorobutylthio and 2,2,2-trichloroethylthio.

In the present invention, C₂-C₆ alkenylthio group indicates a (C₂-C₆ alkenyl)-S— group wherein the alkenyl has the above-mentioned meaning, unless otherwise specified. There can be mentioned, for example, groups such as vinylthio, 1-propenylthio, isopropenylthio, 2-propenylthio, 2-butenylthio, 3-butenylthio, 2-pentenylthio, 3-pentenylthio, 4-pentenylthio, 2-methyl-2-butenylthio, 2,4-pentadienylthio, 2-hexenylthio, 3-hexenylthio, 4-hexenylthio, 5-hexenylthio and 2,4-hexadienylthio.

In the present invention, C₂-C₆ haloalkenylthio group indicates a (C₂-C₆ haloalkenyl)-S— group wherein the haloalkenyl has the above-mentioned meaning, unless otherwise specified. There can be mentioned, for example, groups such as 2,2-difluorovinylthio, 2,2-dichlorovinylthio, 3,3-difluoro-2-propenylthio, 2,3,3-trifluoro-2-propenylthio, 3-chloro-2-propenylthio, 3,3-dichloro-2-propenylthio, 3-bromo-2-propenylthio, 4,4-difluoro-3-butenylthio, 4,4-difluoro-3-butene-2-ylthio, 3,4,4-trifluoro-3-butenylthio, 4,4,4-trifluoro-3-chloro-2-butenylthio, 4,4-dichloro-3-butenylthio, 4,5,5-trifluoro-4-pentenylthio, 5,5,5-trifluoro-3-pentenylthio, 4,4,4-trifluoro-3-trifluoromethyl-2-butenylthio, 6,6-difluoro-5-hexenylthio, 5,6,6-trifluoro-5-hexenylthio and 6,6-dichloro-5-hexenylthio.

In the present invention, C₃-C₆ cycloalkylthio group indicates a (C₃-C₆ cycloalkyl)-S— group wherein the cycloalkyl has the above-mentioned meaning, unless otherwise specified. There can be mentioned, for example, groups such as cyclopropylthio, cyclobutylthio, cyclopentylthio and cyclohexylthio.

In the present invention, C₃-C₆ halocycloalkylthio group indicates a (C₃-C₆ halocycloalkyl)-S— group wherein the halocycloalkyl has the above-mentioned meaning, unless otherwise specified. There can be mentioned, for example, groups such as 2,2-difluorocyclopropylthio, 2,2-dichlorocyclopropylthio, 3,3-difluorocyclobutylthio, 3,3-difluorocyclopentylthio and 4,4-difluorocyclohexylthio.

In the present invention, C₃-C₆ cycloalkyl C₁-C₆ alkylthio group indicates a (C₃-C₆ cycloalkyl)-(C₁-C₆ alkyl)-S— group wherein the cycloalkyl and alkyl has the above-mentioned meaning, unless otherwise specified. There can be mentioned, for example, groups such as cyclopropylmethylthio, 2-cyclopropylethylthio, 3-cyclopropylpropylthio, 4-cyclopropylbutylthio, 5-cyclopropylpentylthio, cyclobutylmethylthio, cyclopentylmethylthio and cyclohexylmethylthio.

In the present invention, C₃-C₆ halocycloalkyl C₁-C₆ alkylthio group indicates a (C₃-C₆ halocycloalkyl)-(C₁-C₆ alkyl)-S— group wherein the halocycloalkyl and alkyl has the above-mentioned meaning, unless otherwise specified. There can be mentioned, for example, groups such as 2,2-difluorocyclopropylmethylthio, 2,2-dichlorocyclopropylmethylthio, 2-(2,2-difluorocyclopropyl)ethylthio, 2-(2,2-dichlorocyclopropyl)ethylthio, 2,2-difluorocyclobutylmethylthio and 4,4-difluorocyclohexylmethylthio.

In the present invention, tri(C₁-C₆ alkyl)silyl-C₁-C₆ alkylthio group indicates a (C₁-C₆ alkyl)₃-Si—(C₁-C₆ alkyl)-S— group wherein the alkyl has the above-mentioned meaning, unless otherwise specified. There can be mentioned, for example, groups such as trimethylsilylmethylthio, triethylsilylmethylthio, trimethylsilylethylthio, tertbutyldimethylsilylmethylthio, and trimethylsilylpropylthio.

In the present invention, C₁-C₆ alkylsulfinyl group indicates a (C₁-C₆ alkyl)-SO— group wherein the alkyl has the above-mentioned meaning, unless otherwise specified. There can be mentioned, for example, groups such as methylsulfinyl, ethylsulfinyl, n-propylsulfinyl, isopropylsulfinyl, n-butylsulfinyl, isobutylsulfinyl, sec-butylsulfinyl and tert-butylsulfinyl.

In the present invention, C₁-C₆ haloalkylsulfinyl group indicates a (C₁-C₆ haloalkyl)-SO— group wherein the haloalkyl has the above-mentioned meaning, unless otherwise specified. There can be mentioned, for example, groups such as difluoromethylsulfinyl, trifluoromethylsulfinyl, 2,2,2-trifluoroethylsulfinyl, 2,2,2-trichloroethylsulfinyl, pentafluoroethylsulfinyl, heptafluoropropylsulfinyl, trichloromethylsulfinyl and heptafluoro-2-propylsulfinyl.

In the present invention, C₃-C₆ cycloalkylsulfinyl group indicates a (C₃-C₆ cycloalkyl)-SO— group wherein the cycloalkyl has the above-mentioned meaning, unless otherwise specified. There can be mentioned, for example, groups such as cyclopropylsulfinyl, cyclobutylsulfinyl, cyclopentylsulfinyl and cyclohexylsulfinyl.

In the present invention, C₃-C₆ halocycloalkylsulfinyl group indicates a (C₃-C₆ halocycloalkyl)-SO— group wherein the halocycloalkyl has the above-mentioned meaning, unless otherwise specified. There can be mentioned, for example, groups such as 2,2-difluorocyclopropylsulfinyl, 2,2-dichlorocyclopropylsulfinyl, 3,3-difluorocyclobutylsulfinyl, 3,3-difluorocyclopentylsulfinyl and 4,4-difluorocyclohexylsulfinyl.

In the present invention, C₁-C₆ alkylsulfonyl group indicates a (C₁-C₆ alkyl)-SO₂— group wherein the alkyl has the above-mentioned meaning, unless otherwise specified. There can be mentioned, for example, groups such as methylsulfonyl, ethylsulfonyl, n-propylsulfonyl, isopropylsulfonyl, n-butylsulfonyl, isobutylsulfonyl, sec-butylsulfonyl and tert-butylsulfonyl.

In the present invention, C₁-C₆ haloalkylsulfonyl group indicates a (C₁-C₆ haloalkyl)-SO₂— group wherein the haloalkyl has the above-mentioned meaning, unless otherwise specified. There can be mentioned, for example, groups such as difluoromethylsulfonyl, trifluoromethylsulfonyl, trichloromethylsulfonyl, 2,2,2-trifluoroethylsulfonyl, 3,3,3-trifluoropropylsulfonyl and heptafluoro-2-propylsulfonyl.

In the present invention, C₃-C₆ cycloalkylsulfonyl group indicates a (C₃-C₆ cycloalkyl)-SO₂— group wherein the cycloalkyl has the above-mentioned meaning, unless otherwise specified. There can be mentioned, for example, groups such as cyclopropylsulfonyl, cyclobutylsulfonyl, cyclopentylsulfonyl and cyclohexylsulfonyl.

In the present invention, C₃-C₆ halocycloalkylsulfonyl group indicates a (C₃-C₆ halocycloalkyl)-SO₂— group wherein the halocycloalkyl has the above-mentioned meaning, unless otherwise specified. There can be mentioned, for example, groups such as 2,2-difluorocyclopropylsulfonyl, 2,2-dichlorocyclopropylsulfonyl, 3,3-difluorocyclobutylsulfonyl, 3,3-difluorocyclopentylsulfonyl and 4,4-difluorocyclohexylsulfonyl.

In the present invention, C₁-C₆ alkylthio C₁-C₆ alkyl group indicates a (C₁-C₆ alkyl)-S—(C₁-C₆ alkyl) group wherein the alkyl has the above-mentioned meaning, unless otherwise specified. There can be mentioned, for example, groups such as methylthiomethyl, 2-(methylthio)ethyl, 3-(methylthio)propyl, 4-(methylthio)butyl, ethylthiomethyl, propylthiomethyl, butylthiomethyl and pentylthiomethyl.

In the present invention, C₁-C₆ haloalkylthio C₁-C₆ alkyl group indicates a (C₂-C₆ haloalkyl)-S—(C₁-C₆ alkyl) group wherein the alkyl and haloalkyl have the above-mentioned meaning, unless otherwise specified. There can be mentioned, for example, groups such as trifluoromethylthiomethyl, difluoromethylthiomethyl, 2,2,2-trifluoroethylthiomethyl, 2,2,2-trichloroethylthiomethyl, 2-(trifluoromethylthio)ethyl, 2-(difluoromethylthio)ethyl, 2-(2,2,2-trifluoroethylthio)ethyl, 3-(trifluoromethylthio)propyl, 3-(difluoromethylthio)propyl and 3-(2,2,2-trifluoroethylthio)propyl.

In the present invention, C₁-C₆ alkylcarbonyl group indicates a (C₁-C₆ alkyl)-C(═O)— group wherein the alkyl has the above-mentioned meaning, unless otherwise specified. There can be mentioned, for example, groups such as acetyl, propionyl, isopropionyl and pivaloyl.

In the present invention, C₁-C₆ haloalkylcarbonyl group indicates a (C₁-C₆ haloalkyl)-C(═O)— group wherein the haloalkyl has the above-mentioned meaning, unless otherwise specified. There can be mentioned, for example, groups such as fluoroacetyl, difluoroacetyl, trifluoroacetyl, chloroacetyl, trichloroacetyl, tribromoacetyl, 3,3,3-trifluoropropionyl, 3,3-difluoropropionyl and 4,4,4-trifluorobutyryl.

In the present invention, C₁-C₆ alkylcarbonyloxy group indicates a (C₁-C₆ alkyl)-C(═O)—O— group wherein the alkyl has the above-mentioned meaning, unless otherwise specified. There can be mentioned, for example, groups such as acetoxy and propionyloxy.

In the present invention, C₁-C₆ haloalkylcarbonyloxy group indicates a (C₁-C₆ haloalkyl)-C(═O)—O— group wherein the haloalkyl has the above-mentioned meaning, unless otherwise specified. There can be mentioned, for example, groups such as fluoroacetoxy, difluoroacetoxy, trifluoroacetoxy, chloroacetoxy, trichloroacetoxy, tribromoacetoxy, 3,3,3-trifluoropropionyloxy, 3,3-difluoropropionyloxy and 4,4,4-trifluorobutyryloxy.

In the present invention, C₁-C₆ alkoxycarbonyl group indicates a (C₁-C₆ alkoxy)-C(═O)— group wherein the alkoxy has the above-mentioned meaning, unless otherwise specified. There can be mentioned, for example, groups such as methoxycarbonyl, ethoxycarbonyl, n-propoxycarbonyl, isopropoxycarbonyl and tert-butoxycarbonyl.

In the present invention, C₁-C₆ haloalkoxycarbonyl group indicates a (C₁-C₆ haloalkoxy)-C(═O)— group wherein the haloalkoxy has the above-mentioned meaning, unless otherwise specified. There can be mentioned, for example, groups such as 2-fluoroethoxycarbonyl, 2,2,2-trifluoroethoxycarbonyl, 2,2,2-trichloroethoxycarbonyl, pentafluoroethoxycarbonyl, 3,3,3-trifluoropropoxycarbonyl and heptafluoro-2-propoxycarbonyl.

In the present invention, C₁-C₆ alkylamino group indicates a (C₁-C₆ alkyl)-NH— group wherein the alkyl has the above-mentioned meaning, unless otherwise specified. There can be mentioned, for example, groups such as methylamino, ethylamino and n-propylamino.

In the present invention, C₁-C₆ haloalkylamino group indicates a (C₁-C₆ haloalkyl)-NH— group wherein the haloalkyl has the above-mentioned meaning, unless otherwise specified. There can be mentioned, for example, groups such as 2-fluoroethylamino, 2,2-difluoroethylamino, 2,2,2-trifluoroethylamino, 2,2,2-trichloroethylamino, pentafluoroethylamino, 3,3,3-trifluoropropylamino and 1,1,1,3,3,3-hexafluoro-2-propylamino.

In the present invention, C₁-C₆ alkylcarbonylamino group indicates a (C₁-C₆ alkyl)-C(═O)—NH— group wherein the alkyl has the above-mentioned meaning, unless otherwise specified. There can be mentioned, for example, groups such as acetylamino, propionylamino, butyrylamino, isobutyrylamino and tert-butylcarbonylamino.

In the present invention, C₁-C₆ haloalkylcarbonylamino group indicates a (C₁-C₆ haloalkyl)-C(═O)—NH— group wherein the haloalkyl has the above-mentioned meaning, unless otherwise specified. There can be mentioned, for example, groups such as fluoroacetylamino, difluoroacetylamino, trifluoroacetylamino, chloroacetylamino, trichloroacetylamino, tribromoacetylamino, 3,3,3-trifluoropropionylamino, pentafluoropropionylamino, 3,3-difluoropropionylamino and 3,3,3-trifluoro-2-methyl-2-trifluoromethylpropionylamino.

In the present invention, C₁-C₆ alkoxycarbonylamino group indicates a (C₁-C₆ alkoxy)-C(═O)—NH— group wherein the alkoxy has the above-mentioned meaning, unless otherwise specified. There can be mentioned, for example, groups such as methoxycarbonylamino, ethoxycarbonylamino, npropoxycarbonylamino and isopropoxycarbonylamino.

In the present invention, C₁-C₆ haloalkoxycarbonylamino group indicates a (C₁-C₆ haloalkoxy)-C(═O)—NH— group wherein the haloalkoxy has the above-mentioned meaning, unless otherwise specified. There can be mentioned, for example, groups such as 2-fluoroethoxycarbonylamino, 2,2,2-trifluoroethoxycarbonylamino, 2,2,2-trichloroethoxycarbonylamino, pentafluoroethoxycarbonylamino, 3,3,3-trifluoropropoxycarbonylamino, and heptafluoro-2-propoxycarbonylamino.

In the present invention, C₁-C₆ alkylaminocarbonylamino group indicates a (C₁-C₆ alkyl)-NH—C(═O)—NH— group wherein the alkyl has the above-mentioned meaning, unless otherwise specified. There can be mentioned, for example, groups such as methylaminocarbonylamino, ethylaminocarbonylamino, n-propylaminocarbonylamino, isopropylaminocarbonylamino, tert-butylaminocarbonylamino, and tertpentylaminocarbonylamino.

In the present invention, C₁-C₆ haloalkylaminocarbonylamino group indicates a (C₁-C₆ haloalkyl)-NH—C(═O)—NH— group wherein the haloalkyl has the above-mentioned meaning, unless otherwise specified. There can be mentioned, for example, groups such as 2-fluoroethylaminocarbonylamino, 2,2,2-trifluoroethylaminocarbonylamino, 2,2,2-trichloroethylaminocarbonylamino, pentafluoroethylaminocarbonylamino and 1,1,1,3,3,3-hexafluoro-2-propylaminocarbonylamino.

In the present invention, C₁-C₆ alkylsulfonylamino group indicates a (C₁-C₆ alkyl)-SO₂—NH— group wherein the alkyl has the above-mentioned meaning, unless otherwise specified. There can be mentioned, for example, groups such as methylsulfonylamino, ethylsulfonylamino, n-propylsulfonylamino, isopropylsulfonylamino and tertbutylsulfonylamino.

In the present invention, C₁-C₆ haloalkylsulfonylamino group indicates a (C₁-C₆ haloalkyl)-SO₂—NH— group wherein the haloalkyl has the above-mentioned meaning, unless otherwise specified. There can be mentioned, for example, groups such as fluoromethylsulfonylamino, difluoromethylsulfonylamino, tri fluoromethylsulfonylamino, chloromethylsulfonylamino, trichloromethylsulfonylamino, 2,2,2-trifluoroethylsulfonylamino, 2,2-difluoroethylsulfonylamino and 3,3,3-trifluoropropylsulfonylamino.

In the present invention, C₁-C₆ alkylaminocarbonylthio group indicates a (C₁-C₆ alkyl)-NH—C(O═)—S— group wherein the alkyl has the above-mentioned meaning, unless otherwise specified. There can be mentioned, for example, groups such as methylaminocarbonylthio, ethylaminocarbonylthio, propylaminocarbonylthio, isopropylaminocarbonylthio and dimethylaminocarbonylthio.

In the present invention, C₁-C₆ haloalkylaminocarbonylthio group indicates a (C₁-C₆ haloalkyl)-NH—C(O═)—S— group wherein the haloalkyl has the above-mentioned meaning, unless otherwise specified. There can be mentioned, for example, groups such as 2-fluoroethylaminocarbonylthio, 2,2,2-trifluoroethylaminocarbonylthio, 2,2,2-trichloroethylaminocarbonylthio, pentafluoroethylaminocarbonylthio and 1,1,1,3,3,3-hexafluoro-2-propylaminocarbonylthio.

In the present invention, C₁-C₆ alkylaminocarbonyl group indicates a (C₁-C₆ alkyl)-NH—C(═O)— group wherein the alkyl has the above-mentioned meaning, unless otherwise specified. There can be mentioned, for example, groups such as methylaminocarbonyl, ethylaminocarbonyl, propylaminocarbonyl and isopropylaminocarbonyl.

In the present invention, C₁-C₆ haloalkylaminocarbonyl group indicates a (C₁-C₆ haloalkyl)-NH—C(═O)— group wherein the haloalkyl has the above-mentioned meaning, unless otherwise specified. There can be mentioned, for example, groups such as 2-fluoroethylaminocarbonyl, 2,2,2-trifluoroethylaminocarbonyl, 2,2,2-trichloroethylaminocarbonyl, pentafluoroethylaminocarbonyl and 1,1,1,3,3,3-hexafluoro-2-propylaminocarbonyl.

In the present invention, tri(C₁-C₆ alkyl)silyl group indicates a (C₁-C₆ alkyl)₃-Si— group wherein the alkyl has the above-mentioned meaning, unless otherwise specified. There can be mentioned, for example, groups such as trimethylsilyl, triethylsilyl, triisopropylsilyl, dimethylisopropylsilyl and tert-butyldimethylsilyl.

In the present invention, phenyl C₁-C₆ alkyl group indicates a phenyl-(C₁-C₆ alkyl)- group wherein the alkyl has the above-mentioned meaning, unless otherwise specified. There can be mentioned, for example, groups such as benzyl, 1-phenylethyl, 2-phenylethyl, 1-phenylpropyl, 2-phenylbutyl and 1-phenylpentyl.

In the present invention, phenyl C₁-C₆ alkoxy group indicates a phenyl-(C₁-C₆ alkoxy)- group wherein the alkoxy has the above-mentioned meaning, unless otherwise specified. There can be mentioned, for example, groups such as phenylmethoxy, 1-phenylethoxy, 2-phenylethoxy, 1-phenylpropoxy, 2-phenylbutoxy and 1-phenylpentoxy.

In the present invention, phenyl C₁-C₆ alkylthio group indicates a phenyl-(C₁-C₆ alkyl)-S— group wherein the alkyl has the above-mentioned meaning, unless otherwise specified. There can be mentioned, for example, groups such as phenylmethylthio, 1-phenylethylthio, 2-phenylethylthio, 1-phenylpropylthio, 2-phenylbutylthio and 1-phenylpentylthio.

In the present invention, phenyl C₁-C₆ alkylsulfinyl group indicates a phenyl-(C₁-C₆ alkyl)-SO— group wherein the alkyl has the above-mentioned meaning, unless otherwise specified. There can be mentioned, for example, groups such as phenylmethylsulfinyl, 1-phenylethylsulfinyl, 2-phenylethylsulfinyl, 1-phenylpropylsulfinyl, 2-phenylbutylsulfinyl and 1-phenylpentylsulfinyl.

In the present invention, phenyl C₁-C₆ alkylsulfonyl group indicates a phenyl-(C₁-C₆ alkyl)-SO₂— group wherein the alkyl has the above-mentioned meaning, unless otherwise specified. There can be mentioned, for example, groups such as phenylmethylsulfonyl, 1-phenylethylsulfonyl, 2-phenylethylsulfonyl, 1-phenylpropylsulfonyl, 2-phenylbutylsulfonyl and 1-phenylpentylsulfonyl.

In the present invention, agriculturally acceptable salt refers, when the present compound represented by the general formula [I] and general formula [I′] contains, in its structure, hydroxyl group, carboxyl group, amino group, etc., to a salt of the present compound with a metal or an organic base, or with a mineral acid or an organic acid. As the metal, there can be mentioned an alkali metal such as sodium, potassium or the like, or an alkaline earth metal such as magnesium, calcium or the like. As the organic base, there can be mentioned triethylamine, diisopropylamine, etc. As the mineral acid, there can be mentioned hydrochloric acid, hydrobromic acid, sulfuric acid, etc. As the organic acid, there can be mentioned formic acid, acetic acid, methanesulfonic acid, 4-toluenesulfonic acid, trifluoromethanesulfonic acid, etc.

Next, representative examples of the compounds included in the alkyl phenyl sulfide derivative represented by the general formula [I] are shown in Table 1 to Table 41, and those represented by the general formula [I′] are shown in Table 42. However, the compounds included in the present derivative are not restricted thereto. Incidentally, the compound Nos. shown in Tables are used in later description.

Incidentally, the compounds included in the alkyl phenyl sulfide derivative of the present invention contain, in some cases, geometrical isomers of E form and Z form depending upon the kinds of substituent groups. The present invention includes the E forms, the Z forms and mixtures containing the E form and the Z form at any ratio. Also, the compounds included in the present invention contain, in some cases, optical isomers having 1 to 2 asymmetric carbon atoms or asymmetric sulfur atoms. The present invention includes all optical isomers, racemic modifications, and diastereomers.

The following expressions used in the Tables of the present specification indicate the following groups.

Me: methyl

Et: ethyl

tBu: tert-butyl

CF₃: trifluoromethyl

Ph(4-CF₃): 4-trifluoromethylphenyl

Ph(2,5-(CF₃)): 2,5-bis(trifluoromethyl)phenyl

Ph(3-F,4-CF₃): 3-fluoro-4-trifluoromethylphenyl

Ac: acetyl

nPropyl: n-propyl

Isopropyl: isopropyl

nButyl: n-butyl

nPentyl: n-pentyl

nHexyl: n-hexyl

nHeptyl: n-heptyl

nOctyl: n-octyl

nNonyl: n-nonyl

nDecyl: n-decyl

TABLE 1 [I]

Compound No. R¹ R² R³ n R⁴ A-0001 CH₂CF₃ Me F 0 Me A-0002 CH₂CF₃ Me F 1 nPropyl A-0003 CH₂CF₃ Cl F 1 nPropyl A-0004 CH₂CF₃ CN F 0 isopropyl A-0005 CH₂CF₃ CN F 1 isopropyl A-0006 CH₂CF₃ Me F 0 isopropyl A-0007 CH₂CF₃ Me F 1 isopropyl A-0008 CH₂CF₃ Me F 1 nButyl A-0009 CH₂CF₃ Cl F 1 nButyl A-0010 CH₂CF₃ CN F 0 nButyl A-0011 CH₂CF₃ CN F 1 nButyl A-0012 CH₂CF₃ CN F 0 nPentyl A-0013 CH₂CF₃ CN F 1 nPentyl A-0014 CH₂CF₃ Me F 0 nHexyl A-0015 CH₂CF₃ Me F 1 nHexyl A-0016 CH₂CF₃ Cl F 1 nHexyl A-0017 CH₂CF₃ CN F 0 nHexyl A-0018 CH₂CF₃ CN F 1 nHexyl A-0019 CH₂CF₃ Me H 1 nHexyl A-0020 CH₂CF₃ Me Cl 1 nHexyl A-0021 CH₂CF₃ Cl Cl 1 nHexyl A-0022 CH₂CF₃ Me F 0 nHeptyl A-0023 CH₂CF₃ Me F 1 nHeptyl A-0024 CH₂CF₃ CN F 0 nHeptyl A-0025 CH₂CF₃ CN F 1 nHeptyl A-0026 CH₂CF₃ Me F 1 nOctyl A-0027 CH₂CF₃ CN F 0 nOctyl A-0028 CH₂CF₃ CN F 1 nOctyl A-0029 CH₂CF₃ Me F 1 nNonyl A-0030 CH₂CF₃ Me F 0 nDecyl

TABLE 2 Compound No. R¹ R² R³ n R⁴ A-0031 CH₂CF₃ Me F 1 nDecyl A-0032 CH₂CF₃ Me F 0 CH₂CH(Me)CH₃ A-0033 CH₂CF₃ Me F 1 CH₂CH(Me)CH₃ A-0034 CH₂CF₃ Cl F 1 CH₂CH(Me)CH₃ A-0035 CH₂CF₃ CN F 0 CH₂CH(Me)CH₃ A-0036 CH₂CF₃ CN F 1 CH₂CH(Me)CH₃ A-0037 CH₂CF₃ Me F 0 CH₂CH₂CH(Me)CH₃ A-0038 CH₂CF₃ Me F 1 CH₂CH₂CH(Me)CH₃ A-0039 CH₂CF₃ CN F 0 CH₂CH₂CH(Me)CH₃ A-0040 CH₂CF₃ CN F 1 CH₂CH₂CH(Me)CH₃ A-0041 CH₂CF₃ Me F 1 CH₂CH(Me)CH₂CH₃ A-0042 CH₂CF₃ Me F 1 CH(Me)CH₂CH₂CH₃ A-0043 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH(Me)CH₃ A-0044 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH(Me)CH₃ A-0045 CH₂CF₃ Me H 1 CH₂CH₂CH₂CH(Me)CH₃ A-0046 CH₂CF₃ CN F 0 CH₂CH₂CH₂CH(Me)CH₃ A-0047 CH₂CF₃ CN F 1 CH₂CH₂CH₂CH(Me)CH₃ A-0048 CH₂CF₃ Me F 1 CH₂CH₂CH(Me)CH₂CH₃ A-0049 CH₂CF₃ Me F 1 CH₂CH(Me)CH₂CH₂CH₃ A-0050 CH₂CF₃ Me F 1 CH(Me)CH₂CH₂CH₂CH₃ A-0051 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂CH(Me)CH₃ A-0052 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH(Me)CH₃ A-0053 CH₂CF₃ Cl F 1 CH₂CH₂CH₂CH₂CH(Me)CH₃ A-0054 CH₂CF₃ Me H 1 CH₂CH₂CH₂CH₂CH(Me)CH₃ A-0055 CH₂CF₃ CN F 0 CH₂CH₂CH₂CH₂CH(Me)CH₃ A-0056 CH₂CF₃ CN F 1 CH₂CH₂CH₂CH₂CH(Me)CH₃ A-0057 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH(Me)CH₂CH₃ A-0058 CH₂CF₃ Me F 1 CH₂CH₂CH(Me)CH₂CH₂CH₃ A-0059 CH₂CF₃ Me F 1 CH₂CH(Me)CH₂CH₂CH₂CH₃ A-0060 CH₂CF₃ Me F 1 CH(Me)CH₂CH₂CH₂CH₂CH₃ A-0061 CH₂CF₃ Cl F 0 CH₂CH₂CH₂CH₂CH₂CH(Me)CH₃ A-0062 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂CH(Me)CH₃ A-0063 CH₂CF₃ Me F 1 CH₂tBu A-0064 CH₂CF₃ CN F 0 CH₂tBu A-0065 CH₂CF₃ CN F 1 CH₂tBu A-0066 CH₂CF₃ Me F 1 CH₂tBu A-0067 CH₂CF₃ Me F 1 CH₂CH₂tBu A-0068 CH₂CF₃ CN F 0 CH₂CH₂tBu A-0069 CH₂CF₃ CN F 1 CH₂CH₂tBu A-0070 CH₂CF₃ Me F 0 CH₂CH₂tBu

TABLE 3 Compound No. R¹ R² R³ n R⁴ A-0071 CH₂CF₃ Me F 1 CH₂CH₂tBu A-0072 CH₂CF₃ Me F 1 CH₂CH(Me)tBu A-0073 CH₂CF₃ Me F 1 CH(Me)CH₂tBu A-0074 CH₂CF₃ Me F 0 CH₂CH₂CH₂tBu A-0075 CH₂CF₃ Me F 1 CH₂CH₂CH₂tBu A-0076 CH₂CF₃ Cl F 0 CH₂CH₂CH₂tBu A-0077 CH₂CF₃ Cl F 1 CH₂CH₂CH₂tBu A-0078 CH₂CF₃ CN F 0 CH₂CH₂CH₂tBu A-0079 CH₂CF₃ CN F 1 CH₂CH₂CH₂tBu A-0080 CH₂CF₃ Me H 1 CH₂CH₂CH₂tBu A-0081 CH₂CF₃ Me F 2 CH₂CH₂CH₂tBu A-0082 CH₂CF₃ Me F 1 CH₂CH₂CH(Me)tBu A-0083 CH₂CF₃ Me F 1 CH₂CH(Me)CH₂tBu A-0084 CH₂CF₃ Me F 1 CH(Me)CH₂CH₂tBu A-0085 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂tBu A-0086 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂tBu A-0087 CH₂CF₃ Cl F 0 CH₂CH₂CH₂CH₂tBu A-0088 CH₂CF₃ Cl F 1 CH₂CH₂CH₂CH₂tBu A-0089 CH₂CF₃ CN F 0 CH₂CH₂CH₂CH₂tBu A-0090 CH₂CF₃ CN F 1 CH₂CH₂CH₂CH₂tBu A-0091 CH₂CF₃ Me H 0 CH₂CH₂CH₂CH₂tBu A-0092 CH₂CF₃ Me H 1 CH₂CH₂CH₂CH₂tBu A-0093 CH₂CF₃ Me Cl 0 CH₂CH₂CH₂CH₂tBu A-0094 CH₂CF₃ Me Cl 1 CH₂CH₂CH₂CH₂tBu A-0095 CH₂CF₃ Me Me 1 CH₂CH₂CH₂CH₂tBu A-0096 CH₂CF₃ Cl Cl 1 CH₂CH₂CH₂CH₂tBu A-0097 CF₃ Me F 1 CH₂CH₂CH₂CH₂tBu A-0098 CHF₂ Me F 1 CH₂CH₂CH₂CH₂tBu A-0099 tBu Me F 1 CH₂CH₂CH₂CH₂tBu A-0100 CH₂tBu Me F 1 CH₂CH₂CH₂CH₂tBu A-0101 CH₂CH(Me)₂ Me F 1 CH₂CH₂CH₂CH₂tBu A-0102 CH₂CH═CCl₂ Me F 1 CH₂CH₂CH₂CH₂tBu A-0103 CH₂CH≡CH Me F 1 CH₂CH₂CH₂CH₂tBu A-0104 CH₂CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂tBu A-0105 CH₂cPr Me F 1 CH₂CH₂CH₂CH₂tBu A-0106 CF₂CF₃ Me F 1 CH₂CH₂CH₂CH₂tBu A-0107 CH₂CHF₂ Me F 1 CH₂CH₂CH₂CH₂tBu A-0108 CH₂CF₃ Cl H 1 CH₂CH₂CH₂CH₂tBu A-0109 CH₂COOMe Me F 1 CH₂CH₂CH₂CH₂tBu A-0110 CH₂CF₃ Me F 2 CH₂CH₂CH₂CH₂tBu

TABLE 4 Compound No. R¹ R² R³ n R⁴ A-0111 CH₂COOH Me F 1 CH₂CH₂CH₂CH₂tBu A-0112 CH₂tBu Me F 0 CH₂CH₂CH₂CH₂tBu A-0113 CH₂CHF₂ Me F 1 CH₂CH₂CH₂CH₂tBu A-0114 CH₂tBu Me F 1 CH₂CH₂CH₂CH₂tBu A-0115 CH₂cPr Me F 0 CH₂CH₂CH₂CH₂tBu A-0116 CH₂CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂tBu A-0117 CH₂cPr Me F 1 CH₂CH₂CH₂CH₂tBu A-0118 CH₂CF₃ Me Me 0 CH₂CH₂CH₂CH₂tBu A-0119 CH₂CF₃ Me Me 1 CH₂CH₂CH₂CH₂tBu A-0120 CH₂CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂tBu A-0121 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH(Me)tBu A-0122 CH₂CF₃ Me F 0 CH₂CH₂CH(Me)CH₂tBu A-0123 CH₂CF₃ Me F 1 CH₂CH₂CH(Me)CH₂tBu A-0124 CH₂CF₃ Me H 1 CH₂CH₂CH(Me)CH₂tBu A-0125 CH₂CF₃ CN F 0 CH₂CH₂CH(Me)CH₂tBu A-0126 CH₂CF₃ CN F 1 CH₂CH₂CH(Me)CH₂tBu A-0127 CH₂CF₃ Me F 1 CH₂CH(Me)CH₂CH₂tBu A-0128 CH₂CF₃ Me F 1 CH(Me)CH₂CH₂CH₂tBu A-0129 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂CH₂tBu A-0130 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂tBu A-0131 CH₂CF₃ Me H 1 CH₂CH₂CH₂CH₂CH₂tBu A-0132 CH₂CF₃ Cl F 0 CH₂CH₂CH₂CH₂CH₂tBu A-0133 CH₂CF₃ Cl F 1 CH₂CH₂CH₂CH₂CH₂tBu A-0134 CH₂CF₃ Cl H 1 CH₂CH₂CH₂CH₂CH₂tBu A-0135 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH(Me)tBu A-0136 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH(Me)CH₂tBu A-0137 CH₂CF₃ Me F 1 CH₂CH₂CH(Me)CH₂CH₂tBu A-0138 CH₂CF₃ Me F 1 CH₂CH(Me)CH₂CH₂CH₂tBu A-0139 CH₂CF₃ Me F 1 CH(Me)CH₂CH₂CH₂CH₂tBu A-0140 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂CH₂CH₂tBu A-0141 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂CH₂tBu A-0142 CH₂CF₃ Me H 1 CH₂CH₂CH₂CH₂CH₂CH₂tBu A-0143 CH₂CF₃ Cl F 0 CH₂CH₂CH₂CH₂CH₂CH₂tBu A-0144 CH₂CF₃ Cl F 1 CH₂CH₂CH₂CH₂CH₂CH₂tBu A-0145 CH₂CF₃ CN F 1 CH₂CH₂CH₂CH₂CH₂CH₂tBu A-0146 CH₂CF₃ Me H 0 CH₂CH₂CH₂CH₂CH₂CH₂tBu A-0147 CH₂CF₃ Me H 1 CH₂CH₂CH₂CH₂CH₂CH₂tBu A-0148 CH₂CF₃ Me Cl 1 CH₂CH₂CH₂CH₂CH₂CH₂tBu A-0149 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂CH(Me)tBu A-0150 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH(Me)CH₂tBu

TABLE 5 Compound No. R¹ R² R³ n R⁴ A-0151 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH(Me)CH₂CH₂tBu A-0152 CH₂CF₃ Me F 1 CH₂CH₂CH(Me)CH₂CH₂CH₂tBu A-0153 CH₂CF₃ Me F 1 CH₂CH(Me)CH₂CH₂CH₂CH₂tBu A-0154 CH₂CF₃ Me F 1 CH(Me)CH₂CH₂CH₂CH₂CH₂tBu A-0155 CH₂CF₃ Me F 1 CH₂CF₃ A-0156 CH₂CF₃ Me F 1 CH(Me)CF₃ A-0157 CH₂CF₃ Me F 1 CH₂CH₂CF₃ A-0158 CH₂CF₃ Cl F 1 CH₂CH₂CF₃ A-0159 CH₂CF₃ Me F 0 CH₂CH₂CH₂CF₃ A-0160 CH₂CF₃ Me F 1 CH₂CH₂CH₂CF₃ A-0161 CH₂CF₃ Cl F 1 CH₂CH₂CH₂CF₃ A-0162 CH₂CF₃ Me H 1 CH₂CH₂CH₂CF₃ A-0163 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂CF₃ A-0164 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CF₃ A-0165 CH₂CF₃ Cl F 1 CH₂CH₂CH₂CH₂CF₃ A-0166 CH₂CF₃ Me H 1 CH₂CH₂CH₂CH₂CF₃ A-0167 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂CH₂CF₃ A-0168 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂CF₃ A-0169 CH₂CF₃ Cl F 0 CH₂CH₂CH₂CH₂CH₂CF₃ A-0170 CH₂CF₃ Cl F 1 CH₂CH₂CH₂CH₂CH₂CF₃ A-0171 CH₂CF₃ Me F 1 CH(CF₃)CF₃ A-0172 CH₂CF₃ Me F 0 CH₂CF₂CF₃ A-0173 CH₂CF₃ Me F 1 CH₂CF₂CF₃ A-0174 CH₂CF₃ Cl F 0 CH₂CF₂CF₃ A-0175 CH₂CF₃ Cl F 1 CH₂CF₂CF₃ A-0176 CH₂CF₃ Me F 1 CH₂CF₂CF₃ A-0177 CH₂CF₃ Me F 1 CH₂CF(CF₃)CF₃ A-0178 CH₂CF₃ Me F 1 CH₂CF₂CF₂CF₃ A-0179 CH₂CF₃ Cl F 1 CH₂CF₂CF₂CF₃ A-0180 CH₂CF₃ CN F 0 CH₂CF₂CF₂CF₃ A-0181 CH₂CF₃ CN F 1 CH₂CF₂CF₂CF₃ A-0182 CH₂CF₃ Me F 1 CH₂CF₂CF(CF₃)CF₃ A-0183 CH₂CF₃ Me F 1 CH₂CF(CF₃)CF₂CF₃ A-0184 CH₂CF₃ Me F 0 CH₂CF₂CF₂CF₂CF₃ A-0185 CH₂CF₃ Me F 1 CH₂CF₂CF₂CF₂CF₃ A-0186 CH₂CF₃ Cl F 0 CH₂CF₂CF₂CF₂CF₃ A-0187 CH₂CF₃ Cl F 1 CH₂CF₂CF₂CF₂CF₃ A-0188 CH₂CF₃ CN F 0 CH₂CF₂CF₂CF₂CF₃ A-0189 CH₂CF₃ CN F 1 CH₂CF₂CF₂CF₂CF₃ A-0190 CH₂CF₃ Me H 1 CH₂CF₂CF₂CF₂CF₃

TABLE 6 Com- pound No. R¹ R² R³ n R⁴ A-0191 CH₂CF₃ Me Cl 1 CH₂CF₂CF₂CF₂CF₃ A-0192 CH₂CF₃ Me F 1 CH₂CF₂CF₂CF(CF₃)CF₃ A-0193 CH₂CF₃ Me F 1 CH₂CF₂CF(CF₃)CF₂CF₃ A-0194 CH₂CF₃ Me F 1 CH₂CF(CF₃)CF₂CF₂CF₃ A-0195 CH₂CF₃ Me F 1 CH₂CH₂CH₂OCHF₂ A-0196 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂OCHF₂ A-0197 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂OCHF₂ A-0198 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂CH₂OCHF₂ A-0199 CH₂CF₃ Me F 0 CH₂CH₂OCH₂CF₃ A-0200 CH₂CF₃ Me F 1 CH₂CH₂OCH₂CF₃ A-0201 CH₂CF₃ Me F 1 CH₂CH₂CH₂OCH₂CF₃ A-0202 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂OCH₂CF₃ A-0203 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂CH₂OCH₂CF₃ A-0204 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂OCH₂CF₃ A-0205 CH₂CF₃ Cl F 0 CH₂CH₂CH₂CH₂CH₂OCH₂CF₃ A-0206 CH₂CF₃ Cl F 1 CH₂CH₂CH₂CH₂CH₂OCH₂CF₃ A-0207 CH₂CF₃ CN F 0 CH₂CH₂CH₂CH₂CH₂OCH₂CF₃ A-0208 CH₂CF₃ CN F 1 CH₂CH₂CH₂CH₂CH₂OCH₂CF₃ A-0209 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂CH₂OCH₂CF₃ A-0210 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂CH₂CH₂OCH₂CF₃ A-0211 CH₂CF₃ Me F 0 CH₂CH₂CH₂OC(CF₃)₃ A-0212 CH₂CF₃ Me F 1 CH₂CH₂CH₂OC(CF₃)₃ A-0213 CH₂CF₃ Cl F 0 CH₂CH₂CH₂OC(CF₃)₃ A-0214 CH₂CF₃ Cl F 1 CH₂CH₂CH₂OC(CF₃)₃ A-0215 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂OC(CF₃)₃ A-0216 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂OC(CF₃)₃ A-0217 CH₂CF₃ Cl F 0 CH₂CH₂CH₂CH₂OC(CF₃)₃ A-0218 CH₂CF₃ Cl F 1 CH₂CH₂CH₂CH₂OC(CF₃)₃ A-0219 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂CH₂OC(CF₃)₃ A-0220 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂OC(CF₃)₃ A-0221 CH₂CF₃ Cl F 0 CH₂CH₂CH₂CH₂CH₂OC(CF₃)₃ A-0222 CH₂CF₃ Cl F 1 CH₂CH₂CH₂CH₂CH₂OC(CF₃)₃ A-0223 CH₂CF₃ OMe F 0 CH₂CH₂CH₂CH₂CH₂OC(CF₃)₃ A-0224 CH₂CF₃ OMe F 1 CH₂CH₂CH₂CH₂CH₂OC(CF₃)₃ A-0225 CH₂CF₃ Cl F 0 CF₂CHFOCF₂CF₂CF₃ A-0226 CH₂CF₃ Cl F 1 CF₂CHFOCF₂CF₂CF₃ A-0227 CH₂CF₃ Me F 0 CH₂CF₂OCF₂CF₂OCF₃ A-0228 CH₂CF₃ Me F 1 CH₂CF₂OCF₂CF₂OCF₃ A-0229 CH₂CF₃ Cl F 0 CH₂CF₂OCF₂CF₂OCF₃ A-0230 CH₂CF₃ Cl F 1 CH₂CF₂OCF₂CF₂OCF₃

TABLE 7 Com- pound No. R¹ R² R³ n R⁴ A-0231 CH₂CF₃ Me F 0 CF₂CHFOCF₂CF(CF₃)OCF₂CF₂CF₃ A-0232 CH₂CF₃ Me F 1 CF₂CHFOCF₂CF(CF₃)OCF₂CF₂CF₃ A-0233 CH₂CF₃ Cl F 0 CF₂CHFOCF₂CF(CF₃)OCF₂CF₂CF₃ A-0234 CH₂CF₃ Cl F 1 CF₂CHFOCF₂CF(CF₃)OCF₂CF₂CF₃ A-0235 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂OcPr A-0236 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂OcPr A-0237 CH₂CF₃ Cl F 0 CH₂CH₂CH₂CH₂OcPen A-0238 CH₂CF₃ Cl F 1 CH₂CH₂CH₂CH₂OcPen A-0239 CH₂CF₃ Me F 1 CH₂CH₂CH═CH₂ A-0240 CH₂CF₃ Me F 1 CH₂CH₂CH≡CH A-0241 CH₂CF₃ Me F 1 CH₂CH₂CH═C(Me)Me A-0242 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH═CH₂ A-0243 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH≡CH A-0244 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH≡CH A-0245 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH═C(Me)Me A-0246 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH═CH₂ A-0247 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH≡CH A-0248 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH═C(Me)Me A-0249 CH₂CF₃ Me F 0 CH₂CH₂CH(Me)CH₂CH₂CH═C(Me)₂ A-0250 CH₂CF₃ Me F 1 CH₂CH₂CH(Me)CH₂CH₂CH═C(Me)₂ A-0251 CH₂CF₃ Me F 0 CH₂CH₂CF═CF₂ A-0252 CH₂CF₃ Me F 1 CH₂CH₂CF═CF₂ A-0253 CH₂CF₃ Me F 0 CH₂CH═C(Cl)CF₃ A-0254 CH₂CF₃ Me F 1 CH₂CH═C(Cl)CF₃ A-0255 CH₂CF₃ Me F 1 CH₂CH₂CH₂CF═CF₂ A-0256 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂CF═CF₂ A-0257 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CF═CF₂ A-0258 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂CF═CF₂ A-0259 CH₂CF₃ Me F 1 CH₂CH═C═CF₂ A-0260 CH₂CF₃ Me F 0 CH₂CH₂CH₂Cl A-0261 CH₂CF₃ Me F 0 CH₂CH₂CH₂Br A-0262 CH₂CF₃ Me F 1 CH₂CH₂CH₂Br A-0263 CH₂CF₃ Cl F 0 CH₂CH₂CH₂Br A-0264 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂Br A-0265 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂Br A-0266 CH₂CF₃ Cl F 0 CH₂CH₂CH₂CH₂Br A-0267 CH₂CF₃ Cl Cl 0 CH₂CH₂CH₂CH₂Br A-0268 CH₂CF₃ Cl F 1 CH₂CH₂CH₂CH₂Br A-0269 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂CH₂Br A-0270 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂Br

TABLE 8 Com- pound No. R¹ R² R³ n R⁴ A-0271 CH₂CF₃ Cl F 0 CH₂CH₂CH₂CH₂CH₂Cl A-0272 CH₂CF₃ Cl F 1 CH₂CH₂CH₂CH₂CH₂Cl A-0273 CH₂CF₃ Cl F 0 CH₂CH₂CH₂CH₂CH₂Br A-0274 CH₂CF₃ Cl F 1 CH₂CH₂CH₂CH₂CH₂Br A-0275 CH₂CF₃ OMe F 0 CH₂CH₂CH₂CH₂CH₂Br A-0276 CH₂CF₃ OMe F 1 CH₂CH₂CH₂CH₂CH₂Br A-0277 CH₂CF₃ CN F 0 CH₂CH₂CH₂CH₂CH₂Cl A-0278 CH₂CF₃ CN F 1 CH₂CH₂CH₂CH₂CH₂Cl A-0279 CH₂CF₃ Me H 0 CH₂CH₂CH₂CH₂CH₂Cl A-0280 CH₂CF₃ Me H 1 CH₂CH₂CH₂CH₂CH₂Cl A-0281 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂CH₂CH₂Br A-0282 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂CH₂Br A-0283 CH₂CF₃ Cl Cl 0 CH₂CH₂CH₂CH₂CH₂CH₂Br A-0284 CH₂CF₃ Me Me 0 CH₂CH₂CH₂CH₂CH₂CH₂Br A-0285 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂CH₂CH₂Cl A-0286 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂CH₂Cl A-0287 CH₂CF₃ Me H 0 CH₂CH₂CH₂CH₂CH₂CH₂Br A-0288 CH₂CF₃ Me H 1 CH₂CH₂CH₂CH₂CH₂CH₂Br A-0289 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂CH₂CH₂CH₂Cl A-0290 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂CH₂CH₂Cl A-0291 CH₂CF₃ Me F 0 CH₂CH₂CH(CH₃)CH₂CH₂Br A-0292 CH₂CF₃ Me F 0 CH₂CH₂OH A-0293 CH₂CF₃ Me F 1 CH₂CH₂OH A-0294 CH₂CF₃ Me H 0 CH₂CH₂OH A-0295 CH₂CF₃ Me F 0 CH₂CH₂CH₂OH A-0296 CH₂CF₃ Me F 1 CH₂CH₂CH₂OH A-0297 CH₂CF₃ Me H 0 CH₂CH₂CH₂OH A-0298 CH₂CF₃ Me H 1 CH₂CH₂CH₂OH A-0299 CH₂CF₃ Cl F 0 CH₂CH₂CH₂CH₂OH A-0300 CH₂CF₃ Cl F 1 CH₂CH₂CH₂CH₂OH A-0301 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂CH₂OH A-0302 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂OH A-0303 CH₂CF₃ Cl F 0 CH₂CH₂CH₂CH₂CH₂OH A-0304 CH₂CF₃ Cl F 1 CH₂CH₂CH₂CH₂CH₂OH A-0305 CH₂CF₃ Me F 0 CH₂CH₂cPr A-0306 CH₂CF₃ Me F 1 CH₂CH₂cPr A-0307 CH₂CF₃ Me F 0 CH₂CH₂cPr(2,2-F₂) A-0308 CH₂CF₃ Me F 1 CH₂CH₂cPr(2,2-F₂) A-0309 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂cPr A-0310 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂cPr

TABLE 9 Compound No. R¹ R² R³ n R⁴ A-0311 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂cPr(2,2-F₂) A-0312 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂cPr(2,2-F₂) A-0313 CH₂CF₃ Me F 1 CH₂cPr(1-Ph) A-0314 CH₂CF₃ Cl F 1 CH₂cPr(1-Ph) A-0315 CH₂CF₃ Me F 0 CH₂cHex(4-tBu) A-0316 CH₂CF₃ Me F 1 CH₂cHex(4-tBu) A-0317 CH₂CF₃ Me F 0 CH₂cHex(4-CF₃) A-0318 CH₂CF₃ Me F 1 CH₂cHex(4-CF₃) A-0319 CH₂CF₃ Me F 0 CH₂cHex(4,4-F₂) A-0320 CH₂CF₃ Me F 1 CH₂cHex(4,4-F₂) A-0321 CH₂CF₃ Cl F 0 CH₂cHex(4,4-F₂) A-0322 CH₂CF₃ Cl F 1 CH₂cHex(4,4-F₂) A-0323 CH₂CF₃ Me F 1 CH₂CH₂cHex A-0324 CH₂CF₃ Me F 0 CH₂CH₂cHex(4-CF₃) A-0325 CH₂CF₃ Cl F 0 CH₂CH₂cHex(4-CF₃) A-0326 CH₂CF₃ Me F 1 CH₂CH₂cHex(4-CF₃) A-0327 CH₂CF₃ Cl F 1 CH₂CH₂cHex(4-CF₃) A-0328 CH₂CF₃ Me F 0 CH₂CH₂cHex(4,4-F₂) A-0329 CH₂CF₃ Cl F 0 CH₂CH₂cHex(4,4-F₂) A-0330 CH₂CF₃ Me F 1 CH₂CH₂cHex(4,4-F₂) A-0331 CH₂CF₃ Cl F 1 CH₂CH₂cHex(4,4-F₂) A-0332 CH₂CF₃ Me F 1 CH₂CH₂cHex(4-SCF₃) A-0333 CH₂CF₃ Cl F 1 CH₂CH₂cHex(4-SCF₃) A-0334 CH₂CF₃ Me F 1 CH₂CH₂cHex(4-SCHF₂) A-0335 CH₂CF₃ Me F 1 CH₂CH₂cHex(4-OCHF₂) A-0336 CH₂CF₃ Me F 1 CH₂CH₂cHex(4-OCF₃) A-0337 CH₂CF₃ Me F 1 CH₂CH₂CH₂cHex A-0338 CH₂CF₃ Me F 0 CH₂CH₂CH₂cHex(4-CF₃) A-0339 CH₂CF₃ Me F 1 CH₂CH₂CH₂cHex(4-CF₃) A-0340 CH₂CF₃ Cl F 0 CH₂CH₂CH₂cHex(4-CF₃) A-0341 CH₂CF₃ Cl F 1 CH₂CH₂CH₂cHex(4-CF₃) A-0342 CH₂CF₃ Me F 0 CH₂CH₂CH₂cHex(4-tBu) A-0343 CH₂CF₃ Me F 1 CH₂CH₂CH₂cHex(4-tBu) A-0344 CH₂CF₃ Me F 1 CH₂CH₂CH₂cHex(4-SCF₃) A-0345 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂cHex A-0346 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂cHex A-0347 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂cHex A-0348 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂cHex(4-CF₃) A-0349 CH₂CF₃ Me F 0 CH₂CH₂(adamant-1-yl) A-0350 CH₂CF₃ Me F 1 CH₂CH₂(adamant-1-yl)

TABLE 10 Compound No. R¹ R² R³ n R⁴ A-0351 CH₂CF₃ Me F 1 CH₂CH₂StBu A-0352 CH₂CF₃ Me F 1 CH₂CH₂CH₂StBu A-0353 CH₂CF₃ Me F 1 CH₂CH₂CH₂SCH₂tBu A-0354 CH₂CF₃ Me Cl 1 CH₂CH₂CH₂SCH₂tBu A-0355 CH₂CF₃ Me F 1 CH₂CH(CH₃)StBu A-0356 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂StBu A-0357 CH₂CF₃ Me F 1 CH₂CH₂CH(CH₃)StBu A-0358 CH₂CF₃ Me F 1 CH₂CH(CH₃)CH₂StBu A-0359 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂SCH₃ A-0360 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂CH₂SCH₃ A-0361 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂SCH(CH₃)₂ A-0362 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂CH₂SCH(CH₃)₂ A-0363 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂CH₂StBu A-0364 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂StBu A-0365 CH₂CF₃ Cl F 0 CH₂CH₂CH₂CH₂CH₂StBu A-0366 CH₂CF₃ Cl F 1 CH₂CH₂CH₂CH₂CH₂StBu A-0367 CH₂CF₃ Me H 1 CH₂CH₂CH₂CH₂CH₂StBu A-0368 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂CH₂SCH₃ A-0369 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂CH₂CH₂SCH₃ A-0370 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂CH₂SCH(CH₃)₂ A-0371 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH(CH₃)StBu A-0372 CH₂CF₃ Me F 1 CH₂CH₂CH(CH₃)CH₂StBu A-0373 CH₂CF₃ Me F 1 CH₂CH(CH₃)CH₂CH₂StBu A-0374 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂CH₂CH₂StBu A-0375 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂CH₂StBu A-0376 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂CH₂CH₂StBu A-0377 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂ScPen A-0378 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂ScHex A-0379 CH₂CF₃ Cl F 0 CH₂CH₂CH₂CH₂CH₂ScPr A-0380 CH₂CF₃ Cl F 1 CH₂CH₂CH₂CH₂CH₂ScPr A-0381 CH₂CF₃ Me F 1 CH₂CH₂CH₂S(═O)Me A-0382 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂S(═O)tBu A-0383 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂S(═O)Me A-0384 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂CH₂S(═O)tBu A-0385 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂S(═O)cPen A-0386 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂S(═O)cHex A-0387 CH₂CF₃ Cl F 0 CH₂CH₂CH₂CH₂CH₂S(═O)cPr A-0388 CH₂CF₃ Cl F 1 CH₂CH₂CH₂CH₂CH₂S(═O)cPr A-0389 CH₂CF₃ Me F 1 CH₂CH₂S(═O)₂Me A-0390 CH₂CF₃ Me F 1 CH₂CH₂CH₂S(═O)₂Me

TABLE 11 Compound No. R¹ R² R³ n R⁴ A-0391 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂S(═O)₂Me A-0392 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂S(═O)₂Me A-0393 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂CH₂S(═O)₂Me A-0394 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂S(═O)₂Me A-0395 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂CH₂S(═O)₂tBu A-0396 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂S(═O)₂tBu A-0397 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂CH₂S(═O)₂Me A-0398 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂CH₂CH₂S(═O)₂Me A-0399 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂CH₂S(═O)₂cPr A-0400 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂S(═O)₂cPr A-0401 CH₂CF₃ Me F 0 CH₂SCF₃ A-0402 CH₂CF₃ Me F 1 CH₂SCF₃ A-0403 CH₂CF₃ Me F 1 CH₂CH₂SCF₃ A-0404 CH₂CF₃ Me H 1 CH₂CH₂SCF₃ A-0405 CH₂CF₃ Me F 0 CH₂CH₂CH₂SCF₃ A-0406 CH₂CF₃ Me F 1 CH₂CH₂CH₂SCF₃ A-0407 CH₂CF₃ Cl F 1 CH₂CH₂CH₂SCF₃ A-0408 CH₂CF₃ Me H 1 CH₂CH₂CH₂SCF₃ A-0409 CH₂CF₃ Me Cl 1 CH₂CH₂CH₂SCF₃ A-0410 CH₂CF₃ Me Me 0 CH₂CH₂CH₂SCF₃ A-0411 CH₂CF₃ Me Me 1 CH₂CH₂CH₂SCF₃ A-0412 CH₂CF₃ Cl Cl 0 CH₂CH₂CH₂SCF₃ A-0413 CH₂CF₃ Cl Cl 1 CH₂CH₂CH₂SCF₃ A-0414 CH₂CF₃ Me F 1 CH₂CH(CH₃)SCF₃ A-0415 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂SCF₃ A-0416 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂SCF₃ A-0417 CH₂CF₃ Cl F 0 CH₂CH₂CH₂CH₂SCF₃ A-0418 CH₂CF₃ Cl F 1 CH₂CH₂CH₂CH₂SCF₃ A-0419 CH₂CF₃ Me H 1 CH₂CH₂CH₂CH₂SCF₃ A-0420 CH₂CF₃ Me Cl 0 CH₂CH₂CH₂CH₂SCF₃ A-0421 CH₂CF₃ Me Cl 1 CH₂CH₂CH₂CH₂SCF₃ A-0422 CH₂CF₃ Me Me 0 CH₂CH₂CH₂CH₂SCF₃ A-0423 CH₂CF₃ Me Me 1 CH₂CH₂CH₂CH₂SCF₃ A-0424 CH₂CF₃ Cl Cl 0 CH₂CH₂CH₂CH₂SCF₃ A-0425 CH₂CF₃ Cl Cl 1 CH₂CH₂CH₂CH₂SCF₃ A-0426 CH₂CF₃ Me F 1 CH₂CH₂CH(CH₃)SCF₃ A-0427 CH₂CF₃ Me F 1 CH₂CH(CH₃)CH₂SCF₃ A-0428 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂SCF₂CF₃ A-0429 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂SCF(CF₃)₂ A-0430 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂SCF(CF₃)₂

TABLE 12 Compound No. R¹ R² R³ n R⁴ A-0431 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂CH₂SCF₃ A-0432 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂SCF₃ A-0433 CH₂CF₃ Cl F 0 CH₂CH₂CH₂CH₂CH₂SCF₃ A-0434 CH₂CF₃ Cl F 1 CH₂CH₂CH₂CH₂CH₂SCF₃ A-0435 CH₂CF₃ Cl F 2 CH₂CH₂CH₂CH₂CH₂SCF₃ A-0436 CH₂CF₃ CN F 0 CH₂CH₂CH₂CH₂CH₂SCF₃ A-0437 CH₂CF₃ CN F 1 CH₂CH₂CH₂CH₂CH₂SCF₃ A-0438 CH₂CF₃ Me H 0 CH₂CH₂CH₂CH₂CH₂SCF₃ A-0439 CH₂CF₃ Me H 1 CH₂CH₂CH₂CH₂CH₂SCF₃ A-0440 CH₂CF₃ Me Cl 0 CH₂CH₂CH₂CH₂CH₂SCF₃ A-0441 CH₂CF₃ Me Cl 1 CH₂CH₂CH₂CH₂CH₂SCF₃ A-0442 CH₂CF₃ Me Me 0 CH₂CH₂CH₂CH₂CH₂SCF₃ A-0443 CH₂CF₃ Me Me 1 CH₂CH₂CH₂CH₂CH₂SCF₃ A-0444 CH₂CF₃ Cl Cl 0 CH₂CH₂CH₂CH₂CH₂SCF₃ A-0445 CH₂CF₃ Cl Cl 1 CH₂CH₂CH₂CH₂CH₂SCF₃ A-0446 CH₂CF₃ Cl H 0 CH₂CH₂CH₂CH₂CH₂SCF₃ A-0447 CH₂CF₃ Cl H 1 CH₂CH₂CH₂CH₂CH₂SCF₃ A-0448 CH₂CF₃ OMe F 0 CH₂CH₂CH₂CH₂CH₂SCF₃ A-0449 CH₂CF₃ OMe F 1 CH₂CH₂CH₂CH₂CH₂SCF₃ A-0450 CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂SCF₃ A-0451 CHF₂ Me F 1 CH₂CH₂CH₂CH₂CH₂SCF₃ A-0452 tBu Me F 1 CH₂CH₂CH₂CH₂CH₂SCF₃ A-0453 CH₂tBu Me F 1 CH₂CH₂CH₂CH₂CH₂SCF₃ A-0454 CH₂CH(Me)₂ Me F 1 CH₂CH₂CH₂CH₂CH₂SCF₃ A-0455 CH₂CH═CCl₂ Me F 1 CH₂CH₂CH₂CH₂CH₂SCF₃ A-0456 CH₂CH═CH Me F 1 CH₂CH₂CH₂CH₂CH₂SCF₃ A-0457 CH₂CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂SCF₃ A-0458 CH₂cPr Me F 1 CH₂CH₂CH₂CH₂CH₂SCF₃ A-0459 CF₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂SCF₃ A-0460 CH₂CHF₂ Me F 1 CH₂CH₂CH₂CH₂CH₂SCF₃ A-0461 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂SCF₂CF₃ A-0462 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂CH₂SCF(CF₃)₂ A-0463 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂SCF(CF₃)₂ A-0464 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH(CH₃) SCF₃ A-0465 CH₂CF₃ Me F 1 CH₂CH₂CH(CH₃)CH₂SCF₃ A-0466 CH₂CF₃ Me F 1 CH₂CH(CH₃)CH₂CH₂SCF₃ A-0467 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂SCF₂CF₃ A-0468 CH₂CF₃ Me F 1 CH₂CH₂CH(SCF₃)CH₂CH₂ A-0469 CH₂CF₃ Me F 1 CH₂CH(SCF₃)CH₂CH₂CH₂ A-0470 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂CH₂CH₂SCF₃

TABLE 13 Compound No. R¹ R² R³ n R⁴ A-0471 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂CH₂SCF₃ A-0472 CH₂CF₃ Cl F 0 CH₂CH₂CH₂CH₂CH₂CH₂SCF₃ A-0473 CH₂CF₃ Cl F 1 CH₂CH₂CH₂CH₂CH₂CH₂SCF₃ A-0474 CH₂CF₃ Me H 0 CH₂CH₂CH₂CH₂CH₂CH₂SCF₃ A-0475 CH₂CF₃ Me H 1 CH₂CH₂CH₂CH₂CH₂CH₂SCF₃ A-0476 CH₂CF₃ Me Cl 0 CH₂CH₂CH₂CH₂CH₂CH₂SCF₃ A-0477 CH₂CF₃ Me Cl 1 CH₂CH₂CH₂CH₂CH₂CH₂SCF₃ A-0478 CH₂CF₃ Cl Cl 0 CH₂CH₂CH₂CH₂CH₂CH₂SCF₃ A-0479 CH₂CF₃ Cl Cl 1 CH₂CH₂CH₂CH₂CH₂CH₂SCF₃ A-0480 CH₂CF₃ Me Me 0 CH₂CH₂CH₂CH₂CH₂CH₂SCF₃ A-0481 CH₂CF₃ Me Me 1 CH₂CH₂CH₂CH₂CH₂CH₂SCF₃ A-0482 CH₂CHF₂ Me F 0 CH₂CH₂CH₂CH₂CH₂CH₂SCF₃ A-0483 CH₂CHF₂ Me F 1 CH₂CH₂CH₂CH₂CH₂CH₂SCF₃ A-0484 CH₂CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂CH₂CH₂SCF₃ A-0485 CH₂CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂CH₂SCF₃ A-0486 CH₂cPr Me F 0 CH₂CH₂CH₂CH₂CH₂CH₂SCF₃ A-0487 CH₂cPr Me F 1 CH₂CH₂CH₂CH₂CH₂CH₂SCF₃ A-0488 CH₂tBu Me F 0 CH₂CH₂CH₂CH₂CH₂CH₂SCF₃ A-0489 CH₂tBu Me F 1 CH₂CH₂CH₂CH₂CH₂CH₂SCF₃ A-0490 CH₂C≡CH Me F 1 CH₂CH₂CH₂CH₂CH₂CH₂SCF₃ A-0491 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂CH₂CH₂SCF(CF₃)₂ A-0492 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂CH₂SCF(CF₃)₂ A-0493 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH(CH₃)SCF₃ A-0494 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH(CH₃)CH₂SCF₃ A-0495 CH₂CF₃ Me F 0 CH₂CH₂CH(CH₃)CH₂CH₂SCF₃ A-0496 CH₂CF₃ Me F 1 CH₂CH₂CH(CH₃)CH₂CH₂SCF₃ A-0497 CH₂CF₃ Me F 1 CH₂CH(CH₃)CH₂CH₂CH₂SCF₃ A-0498 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂CH₂SCF₂CF₃ A-0499 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH(SCF₃)CH₂CH₃ A-0500 CH₂CF₃ Me F 1 CH₂CH₂CH(SCF₃)CH₂CH₂CH₂ A-0501 CH₂CF₃ Me F 1 CH₂CH(SCF₃)CH₂CH₂CH₂CH₂ A-0502 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂CH₂CH₂CH₂SCF₃ A-0503 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂CH₂CH₂SCF₃ A-0504 CH₂CF₃ Cl F 0 CH₂CH₂CH₂CH₂CH₂CH₂CH₂SCF₃ A-0505 CH₂CF₃ Cl F 1 CH₂CH₂CH₂CH₂CH₂CH₂CH₂SCF₃ A-0506 CH₂CF₃ Me H 1 CH₂CH₂CH₂CH₂CH₂CH₂CH₂SCF₃ A-0507 CH₂CF₃ Me Cl 0 CH₂CH₂CH₂CH₂CH₂CH₂CH₂SCF₃ A-0508 CH₂CF₃ Me Cl 1 CH₂CH₂CH₂CH₂CH₂CH₂CH₂SCF₃ A-0509 CH₂CF₃ Cl Cl 0 CH₂CH₂CH₂CH₂CH₂CH₂CH₂SCF₃ A-0510 CH₂CF₃ Cl Cl 1 CH₂CH₂CH₂CH₂CH₂CH₂CH₂SCF₃

Compound No. R¹ R² R³ n R⁴ A-0511 CH₂CF₃ Me Me 0 CH₂CH₂CH₂CH₂CH₂CH₂CH₂SCF₃ A-0512 CH₂CF₃ Me Me 1 CH₂CH₂CH₂CH₂CH₂CH₂CH₂SCF₃ A-0513 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂CH(CH₃)SCF₃ A-0514 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH(CH₃)CH₂SCF₃ A-0515 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH(CH₃)CH₂CH₂SCF₃ A-0516 CH₂CF₃ Me F 1 CH₂CH₂CH(CH₃)CH₂CH₂CH₂SCF₃ A-0517 CH₂CF₃ Me F 1 CH₂CH(CH₃)CH₂CH₂CH₂CH₂SCF₃ A-0518 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂CH₂CH₂SCF₂CF₃ A-0519 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂CH₂CH₂SCF(CF₃)₂ A-0520 CH₂CF₃ Me F 1 CH₂CH₂CH₂S(═O)CF₃ A-0521 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂S(═O)CF₃ A-0522 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂S(═O)CF₃ A-0523 CH₂CF₃ Cl F 0 CH₂CH₂CH₂CH₂CH₂S(═O)CF₃ A-0524 CH₂CF₃ Cl F 1 CH₂CH₂CH₂CH₂CH₂S(═O)CF₃ A-0525 CH₂CF₃ Cl F 2 CH₂CH₂CH₂CH₂CH₂S(═O)CF₃ A-0526 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂CH₂S(═O)CF₃ A-0527 CH₂CF₃ Cl F 1 CH₂CH₂CH₂CH₂CH₂CH₂S(═O)CF₃ A-0528 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂CH₂CH₂S(═O)CF₃ A-0529 CH₂CF₃ Me F 1 CH₂CH₂CH₂S(═O)₂CF₃ A-0530 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂S(═O)₂CF₃ A-0531 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂S(═O)₂CF₃ A-0532 CH₂CF₃ Cl F 0 CH₂CH₂CH₂CH₂CH₂S(═O)₂CF₃ A-0533 CH₂CF₃ Cl F 1 CH₂CH₂CH₂CH₂CH₂S(═O)₂CF₃ A-0534 CH₂CF₃ Cl F 2 CH₂CH₂CH₂CH₂CH₂S(═O)₂CF₃ A-0535 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂CH₂CH₂S(═O)₂CF₃ A-0536 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂CH₂S(═O)₂CF₃ A-0537 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂CH₂CH₂S(═O)₂CF₃ A-0538 CH₂CF₃ Me F 1 CH₂CH₂SCHF₂ A-0539 CH₂CF₃ Me F 1 CH₂CH₂CH₂SCHF₂ A-0540 CH₂CF₃ Cl F 1 CH₂CH₂CH₂SCHF₂ A-0541 CH₂CF₃ Me H 1 CH₂CH₂CH₂SCHF₂ A-0542 CH₂CF₃ Me F 1 CH₂CH(CH₃)SCHF₂ A-0543 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂SCHF₂ A-0544 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂SCHF₂ A-0545 CH₂CF₃ Cl F 1 CH₂CH₂CH₂CH₂SCHF₂ A-0546 CH₂CF₃ Me H 1 CH₂CH₂CH₂CH₂SCHF₂ A-0547 CH₂CF₃ Me Cl 1 CH₂CH₂CH₂CH₂SCHF₂ A-0548 CH₂CF₃ Cl Cl 1 CH₂CH₂CH₂CH₂SCHF₂ A-0549 CH₂CF₃ Me Me 1 CH₂CH₂CH₂CH₂SCHF₂ A-0550 CH₂CF₃ Me F 1 CH₂CH₂CH(CH₃)SCHF₂

TABLE 15 Compound No. R¹ R² R³ n R⁴ A-0551 CH₂CF₃ Me F 1 CH₂CH(CH₃)CH₂SCHF₂ A-0552 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂SCH₂CHF₂ A-0553 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂CH₂SCHF₂ A-0554 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂SCHF₂ A-0555 CH₂CF₃ Cl F 0 CH₂CH₂CH₂CH₂CH₂SCHF₂ A-0556 CH₂CF₃ Cl F 1 CH₂CH₂CH₂CH₂CH₂SCHF₂ A-0557 CH₂CF₃ Me H 0 CH₂CH₂CH₂CH₂CH₂SCHF₂ A-0558 CH₂CF₃ Me H 1 CH₂CH₂CH₂CH₂CH₂SCHF₂ A-0559 CH₂CF₃ Cl H 1 CH₂CH₂CH₂CH₂CH₂SCHF₂ A-0560 CH₂CF₃ Cl Cl 1 CH₂CH₂CH₂CH₂CH₂SCHF₂ A-0561 CH₂CF₃ Cl Cl 0 CH₂CH₂CH₂CH₂CH₂SCHF₂ A-0562 CH₂CF₃ Me Cl 1 CH₂CH₂CH₂CH₂CH₂SCHF₂ A-0563 CH₂CF₃ Me Me 1 CH₂CH₂CH₂CH₂CH₂SCHF₂ A-0564 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH(CH₃)SCHF₂ A-0565 CH₂CF₃ Me F 1 CH₂CH₂CH(CH₃)CH₂SCHF₂ A-0566 CH₂CF₃ Me F 1 CH₂CH(CH₃)CH₂CH₂SCHF₂ A-0567 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂SCH₂CHF₂ A-0568 CH₂CF₃ Me F 1 CH₂CH₂CH(SCHF₂)CH₂CH₂ A-0569 CH₂CF₃ Me F 1 CH₂CH(SCHF₂)CH₂CH₂CH₂ A-0570 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂CH₂CH₂SCHF₂ A-0571 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂CH₂SCHF₂ A-0572 CH₂CF₃ Cl F 0 CH₂CH₂CH₂CH₂CH₂CH₂SCHF₂ A-0573 CH₂CF₃ Cl F 1 CH₂CH₂CH₂CH₂CH₂CH₂SCHF₂ A-0574 CH₂CF₃ Me H 1 CH₂CH₂CH₂CH₂CH₂CH₂SCHF₂ A-0575 CH₂CF₃ Cl H 1 CH₂CH₂CH₂CH₂CH₂CH₂SCHF₂ A-0576 CH₂CF₃ Me Cl 1 CH₂CH₂CH₂CH₂CH₂CH₂SCHF₂ A-0577 CH₂CF₃ Cl Cl 1 CH₂CH₂CH₂CH₂CH₂CH₂SCHF₂ A-0578 CH₂CF₃ Me Me 1 CH₂CH₂CH₂CH₂CH₂CH₂SCHF₂ A-0579 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH(CH₃)SCHF₂ A-0580 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH(CH₃)CH₂SCHF₂ A-0581 CH₂CF₃ Me F 1 CH₂CH₂CH(CH₃)CH₂CH₂SCHF₂ A-0582 CH₂CF₃ Me F 1 CH₂CH(CH₃)CH₂CH₂CH₂SCHF₂ A-0583 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH(SCHF₂)CH₂CH₂ A-0584 CH₂CF₃ Me F 1 CH₂CH₂CH(SCHF₂)CH₂CH₂CH₂ A-0585 CH₂CF₃ Me F 1 CH₂CH(SCHF₂)CH₂CH₂CH₂CH₂ A-0586 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂CH₂SCH₂CHF₂ A-0587 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂CH₂CH₂SCHF₂ A-0588 CH₂CF₃ Cl F 0 CH₂CH₂CH₂CH₂CH₂CH₂CH₂SCHF₂ A-0589 CH₂CF₃ Cl F 1 CH₂CH₂CH₂CH₂CH₂CH₂CH₂SCHF₂ A-0590 CH₂CF₃ Cl Cl 1 CH₂CH₂CH₂CH₂CH₂CH₂CH₂SCHF₂

TABLE 16 Compound No. R¹ R² R³ n R⁴ A-0591 CH₂CF₃ Me Cl 1 CH₂CH₂CH₂CH₂CH₂CH₂CH₂SCHF₂ A-0592 CH₂CF₃ Me H 1 CH₂CH₂CH₂CH₂CH₂CH₂CH₂SCHF₂ A-0593 CH₂CF₃ Me Me 1 CH₂CH₂CH₂CH₂CH₂CH₂CH₂SCHF₂ A-0594 CH₂CF₃ Me F 1 CH₂CH₂CH₂S(═O)CHF₂ A-0595 CH₂CF₃ Me F 1 CH(CH₃)CH₂S(═O)CHF₂ A-0596 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂S(═O)CHF₂ A-0597 CH₂CF₃ Me F 1 CH₂CH₂CH(CH₃)S(═O)CHF₂ A-0598 CH₂CF₃ Me F 1 CH₂CH(CH₃)CH₂S(═O)CHF₂ A-0599 CH₂CF₃ Cl F 1 CH₂CH₂CH₂CH₂CH₂S(═O)CHF₂ A-0600 CH₂CF₃ Me H 1 CH₂CH₂CH₂CH₂CH₂S(═O)CHF₂ A-0601 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH(CH₃)S(═O)CHF₂ A-0602 CH₂CF₃ Me F 1 CH₂CH₂CH(CH₃)CH₂S(═O)CHF₂ A-0603 CH₂CF₃ Me F 1 CH₂CH(CH₃)CH₂CH₂S(═O)CHF₂ A-0604 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂CH₂S(═O)CHF₂ A-0605 CH₂CF₃ Cl F 1 CH₂CH₂CH₂CH₂CH₂CH₂S(═O)CHF₂ A-0606 CH₂CF₃ Me Cl 1 CH₂CH₂CH₂CH₂CH₂CH₂S(═O)CHF₂ A-0607 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂CH₂CH₂S(═O)CHF₂ A-0608 CH₂CF₃ Me F 1 CH₂CH₂CH₂S(═O)₂CHF₂ A-0609 CH₂CF₃ Me F 1 CH(CH₃)CH₂S(═O)₂CHF₂ A-0610 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂S(═O)₂CHF₂ A-0611 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂S(═O)₂CHF₂ A-0612 CH₂CF₃ Cl F 1 CH₂CH₂CH₂CH₂S(═O)₂CHF₂ A-0613 CH₂CF₃ Me F 1 CH₂CH₂CH(CH₃)S(═O₎₂CHF₂ A-0614 CH₂CF₃ Me F 1 CH₂CH(CH₃)CH₂S(═O)₂CHF₂ A-0615 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂CH₂S(═O)₂CHF₂ A-0616 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂S(═O)₂CHF₂ A-0617 CH₂CF₃ Cl F 0 CH₂CH₂CH₂CH₂CH₂S(═O)₂CHF₂ A-0618 CH₂CF₃ Cl F 1 CH₂CH₂CH₂CH₂CH₂S(═O)₂CHF₂ A-0619 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH(CH₃)S(═O)₂CHF₂ A-0620 CH₂CF₃ Me F 1 CH₂CH₂CH(CH₃)CH₂S(═O)₂CHF₂ A-0621 CH₂CF₃ Me F 1 CH₂CH(CH₃)CH₂CH₂S(═O)₂CHF₂ A-0622 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂CH₂CH₂S(═O)₂CHF₂ A-0623 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂CH₂S(═O)₂CHF₂ A-0624 CH₂CF₃ Me F 1 CH₂CH₂SCH₂CF₃ A-0625 CH₂CF₃ Me F 1 CH₂CH₂CH₂SCH₂CF₃ A-0626 CH₂CF₃ Me H 1 CH₂CH₂CH₂SCH₂CF₃ A-0627 CH₂CF₃ Me F 1 CH₂CH(CH₃)SCH₂CF₃ A-0628 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂SCH₂CF₃ A-0629 CH₂CF₃ Cl F 1 CH₂CH₂CH₂CH₂SCH₂CF₃ A-0630 CH₂CF₃ Me H 1 CH₂CH₂CH₂CH₂SCH₂CF₃

TABLE 17 Compound No. R¹ R² R³ n R⁴ A-0631 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂SCH₂CF₃ A-0632 CH₂CF₃ Cl F 1 CH₂CH₂CH₂CH₂SCH₂CF₃ A-0633 CH₂CF₃ Me Cl 1 CH₂CH₂CH₂CH₂SCH₂CF₃ A-0634 CH₂CF₃ Cl Cl 1 CH₂CH₂CH₂CH₂SCH₂CF₃ A-0635 CH₂CF₃ Me Me 1 CH₂CH₂CH₂CH₂SCH₂CF₃ A-0636 CH₂CF₃ Me F 1 CH₂CH₂CH(CH₃)SCH₂CF₃ A-0637 CH₂CF₃ Me F 1 CH₂CH(CH₃)CH₂SCH₂CF₃ A-0638 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂SCH₂CF₃ A-0639 CH₂CF₃ Cl F 1 CH₂CH₂CH₂CH₂CH₂SCH₂CF₃ A-0640 CH₂CF₃ Me H 1 CH₂CH₂CH₂CH₂CH₂SCH₂CF₃ A-0641 CH₂CF₃ Me Cl 1 CH₂CH₂CH₂CH₂CH₂SCH₂CF₃ A-0642 CH₂CF₃ Cl Cl 1 CH₂CH₂CH₂CH₂CH₂SCH₂CF₃ A-0643 CH₂CF₃ Me Me 1 CH₂CH₂CH₂CH₂CH₂SCH₂CF₃ A-0644 CH₂CF₃ Cl H 1 CH₂CH₂CH₂CH₂CH₂SCH₂CF₃ A-0645 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH(CH₃)SCH₂CF₃ A-0646 CH₂CF₃ Me F 1 CH₂CH₂CH(CH₃)CH₂SCH₂CF₃ A-0647 CH₂CF₃ Me F 1 CH₂CH(CH₃)CH₂CH₂SCH₂CF₃ A-0648 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂CH₂SCH₂CF₃ A-0649 CH₂CF₃ Cl F 1 CH₂CH₂CH₂CH₂CH₂CH₂SCH₂CF₃ A-0650 CH₂CF₃ Me Cl 1 CH₂CH₂CH₂CH₂CH₂CH₂SCH₂CF₃ A-0651 CH₂CF₃ Cl Cl 1 CH₂CH₂CH₂CH₂CH₂CH₂SCH₂CF₃ A-0652 CH₂CF₃ Me Me 1 CH₂CH₂CH₂CH₂CH₂CH₂SCH₂CF₃ A-0653 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH(CH₃)SCH₂CF₃ A-0654 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH(CH₃)CH₂SCH₂CF₃ A-0655 CH₂CF₃ Me F 1 CH₂CH(CH₃)CH₂CH₂CH₂SCH₂CF₃ A-0656 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂CH₂CH₂SCH₂CF₃ A-0657 CH₂CF₃ Me F 1 CH₂CH₂CH₂SCH(CF₃)₂ A-0658 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂SCH(CF₃)₂ A-0659 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂SCH(CF₃)₂ A-0660 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂CH₂SCH(CF₃)₂ A-0661 CH₂CF₃ Cl F 0 CH₂CH₂CH₂CH₂CH₂SCCl₃ A-0662 CH₂CF₃ Cl F 1 CH₂CH₂CH₂CH₂CH₂SCCl₃ A-0663 CH₂CF₃ Me F 0 CH₂CH₂CH₂SCN A-0664 CH₂CF₃ Me Me 0 CH₂CH₂CH₂SCN A-0665 CH₂CF₃ Cl F 0 CH₂CH₂CH₂CH₂SCN A-0666 CH₂CF₃ Me Me 0 CH₂CH₂CH₂CH₂SCN A-0667 CH₂CF₃ Cl Cl 0 CH₂CH₂CH₂CH₂SCN A-0668 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂CH₂SCN A-0669 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂SCN A-0670 CH₂CF₃ Cl F 0 CH₂CH₂CH₂CH₂CH₂SCN

TABLE 18 Compound No. R¹ R² R³ n R⁴ A-0671 CH₂CF₃ CN F 0 CH₂CH₂CH₂CH₂CH₂SCN A-0672 CH₂CF₃ Me H 0 CH₂CH₂CH₂CH₂CH₂SCN A-0673 CH₂CF₃ OMe F 0 CH₂CH₂CH₂CH₂CH₂SCN A-0674 CH₂CF₃ Me F 0 CH₂CH₂CH(Me)CH₂CH₂SCN A-0675 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂CH₂CH₂SCN A-0676 CH₂CF₃ Cl F 0 CH₂CH₂CH₂CH₂CH₂CH₂SCN A-0677 CH₂CF₃ Me H 0 CH₂CH₂CH₂CH₂CH₂CH₂SCN A-0678 CH₂CF₃ Cl Cl 0 CH₂CH₂CH₂CH₂CH₂CH₂SCN A-0679 CH₂CF₃ Me Me 0 CH₂CH₂CH₂CH₂CH₂CH₂SCN A-0680 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂CH₂CH₂CH₂SCN A-0681 CH₂CF₃ Me Me 0 CH₂CH₂CH₂CH₂CH₂CH₂CH₂SCN A-0682 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂SCH₂SiMe₃ A-0683 CH₂CF₃ Me F 1 CH₂CH₂CH₂SCF═CFCF₃ A-0684 CH₂CF₃ Me F 0 CH₂Ph A-0685 CH₂CF₃ Me F 0 CH(Me)Ph A-0686 CH₂CF₃ Me F 1 CH₂Ph A-0687 CH₂CF₃ Me F 0 CH₂Ph(2-CF₃) A-0688 CH₂CF₃ Me F 1 CH₂Ph(2-CF₃) A-0689 CH₂CF₃ Me F 0 CH₂Ph(3-CF₃) A-0690 CH₂CF₃ Me F 0 CH₂Ph(4-CF₃) A-0691 CH₂CF₃ Me F 0 CH(Me)Ph(4-CF₃) A-0692 CH₂CF₃ Me F 1 CH₂Ph(4-CF₃) A-0693 CH₂CF₃ Cl F 0 CH₂Ph(4-CF₃) A-0694 CH₂CF₃ Cl F 1 CH₂Ph(4-CF₃) A-0695 CH₂CF₃ Me Cl 0 CH₂Ph(4-CF₃) A-0696 CH₂CF₃ Me Cl 1 CH₂Ph(4-CF₃) A-0697 CH₂CF₃ CN H 0 CH₂Ph(4-CF₃) A-0698 CH₂CF₃ CN H 1 CH₂Ph(4-CF₃) A-0699 CH₂CF₃ Me F 0 CH₂Ph(2,5-(CF₃)₂) A-0700 CH₂CF₃ Me F 1 CH₂Ph(2,5-(CF₃)₂) A-0701 CH₂CF₃ Me F 1 CH₂Ph(4-OCHF₂) A-0702 CH₂CF₃ Me F 1 CH₂Ph(2-OCF₃) A-0703 CH₂CF₃ Me F 1 CH₂Ph(3-OCF₃) A-0704 CH₂CF₃ Me F 1 CH₂Ph(4-OCF₃) A-0705 CH₂CF₃ Me F 1 CH₂Ph(4-SCHF₂) A-0706 CH₂CF₃ Me F 1 CH₂Ph(2-SCF₃) A-0707 CH₂CF₃ Me F 0 CH₂Ph(3-SCF₃) A-0708 CH₂CF₃ Me F 1 CH₂Ph(3-SCF₃) A-0709 CH₂CF₃ Cl F 0 CH₂Ph(4-SCF₃) A-0710 CH₂CF₃ Cl F 1 CH₂Ph(4-SCF₃)

TABLE 19 Compound No. R¹ R² R³ n R⁴ A-0711 CH₂CF₃ Me F 0 CH₂Ph(4-SCF₃) A-0712 CH₂CF₃ Me F 1 CH₂Ph(4-SCF₃) A-0713 CH₂CF₃ Me F 1 CH₂Ph(3-CH₂SCF₃) A-0714 CH₂CF₃ Me F 1 CH₂Ph(4-CH₂SCF₃) A-0715 CH₂CF₃ Me F 0 CH₂Ph(4-F) A-0716 CH₂CF₃ Me F 0 CH₂Ph(4-Cl) A-0717 CH₂CF₃ Me F 1 CH₂Ph(4-Cl) A-0718 CH₂CF₃ Me F 0 CH₂Ph(4-Br) A-0719 CH₂CF₃ Me F 1 CH₂Ph(4-Br) A-0720 CH₂CF₃ Me F 0 CH₂Ph(4-Me) A-0721 CH₂CF₃ Me F 1 CH₂Ph(4-Me) A-0722 CH₂CF₃ Me F 0 CH₂Ph(4-tBu) A-0723 CH₂CF₃ Me F 1 CH₂Ph(4-tBu) A-0724 CH₂CF₃ Me F 0 CH₂Ph(4-CN) A-0725 CH₂CF₃ Me F 1 CH₂Ph(4-CN) A-0726 CH₂CF₃ Me F 0 CH₂Ph(4-NO₂) A-0727 CH₂CF₃ Me F 1 CH₂Ph(4-NO₂) A-0728 CH₂CF₃ Me F 0 CH₂Ph(2,4-Cl₂) A-0729 CH₂CF₃ Me F 1 CH₂Ph(2,4-Cl₂) A-0730 CH₂CF₃ Me F 0 CH₂Ph(3,4-Cl₂) A-0731 CH₂CF₃ Me F 1 CH₂Ph(3,4-Cl₂) A-0732 CH₂CF₃ Me F 0 CH₂Ph(2,4,6-F₃) A-0733 CH₂CF₃ Me F 1 CH₂Ph(2,4,6-F₃) A-0734 CH₂CF₃ Me F 0 CH₂Ph(3,4,5-F₃) A-0735 CH₂CF₃ Me F 1 CH₂Ph(3,4,5-F₃) A-0736 CH₂CF₃ Me F 1 CH₂Ph(2,3,4-F₃) A-0737 CH₂CF₃ Me F 0 CH₂Ph(2,3,4-Cl₃) A-0738 CH₂CF₃ Me F 0 CH₂Ph(3,4,5-Cl₃) A-0739 CH₂CF₃ Me F 0 CH₂Ph(3,4,5-Cl₃) A-0740 CH₂CF₃ Me F 1 CH₂Ph(3,4,5-Cl₃) A-0741 CH₂CF₃ Me F 0 CH₂Ph(3-CF₃, 4-Cl) A-0742 CH₂CF₃ Me F 1 CH₂Ph(3-CF₃, 4-Cl) A-0743 CH₂CF₃ Me F 0 CH₂Ph(3-CF₃, 4-F) A-0744 CH₂CF₃ Me F 1 CH₂Ph(3-CF₃, 4-F) A-0745 CH₂CF₃ Me F 0 CH₂Ph(3-F, 4-CF₃) A-0746 CH₂CF₃ Me F 1 CH₂Ph(3-F, 4-CF₃) A-0747 CH₂CF₃ Me F 0 CH₂Ph(4-CF(CF₃)₂) A-0748 CH₂CF₃ Me F 1 CH₂Ph(4-CF(CF₃)₂) A-0749 CH₂CF₃ Me F 1 CH₂Ph(4-CH₂SCF₃) A-0750 CH₂CF₃ Me F 0 CH₂Ph(4-Ph(4-CF₃))

TABLE 20 Compound No. R¹ R² R³ n R⁴ A-0751 CH₂CF₃ Me F 0 CH₂CH₂Ph A-0752 CH₂CF₃ Me F 1 CH₂CH₂Ph A-0753 CH₂CF₃ Me F 0 CH₂CH₂Ph(4-F) A-0754 CH₂CF₃ Me F 1 CH₂CH₂Ph(4-F) A-0755 CH₂CF₃ Me F 0 CH₂CH₂Ph(4-Cl) A-0756 CH₂CF₃ Me F 1 CH₂CH₂Ph(4-Cl) A-0757 CH₂CF₃ Me F 0 CH₂CH₂Ph(4-Br) A-0758 CH₂CF₃ Me F 1 CH₂CH₂Ph(4-Br) A-0759 CH₂CF₃ Me F 0 CH₂CH₂Ph(2-CF₃) A-0760 CH₂CF₃ Me F 1 CH₂CH₂Ph(2-CF₃) A-0761 CH₂CF₃ Me F 0 CH₂CH₂Ph(3-CF₃) A-0762 CH₂CF₃ Me F 1 CH₂CH₂Ph(3-CF₃) A-0763 CH₂CF₃ Me F 0 CH₂CH₂Ph(4-CF₃) A-0764 CH₂CF₃ Me F 1 CH₂CH₂Ph(4-CF₃) A-0765 CH₂CF₃ Cl F 0 CH₂CH₂Ph(4-CF₃) A-0766 CH₂CF₃ Cl F 1 CH₂CH₂Ph(4-CF₃) A-0767 CH₂CF₃ Cl Cl 1 CH₂CH₂Ph(4-CF₃) A-0768 CH₂CF₃ Me Me 1 CH₂CH₂Ph(4-CF₃) A-0769 CH₂CF₃ Me Cl 1 CH₂CH₂Ph(4-CF₃) A-0770 tBu CN F 0 CH₂CH₂Ph(4-CF₃) A-0771 tBu CN F 1 CH₂CH₂Ph(4-CF₃) A-0772 CH₂CF₃ Cl F 0 CH₂CH₂Ph(4-OCHF₂) A-0773 CH₂CF₃ Cl F 1 CH₂CH₂Ph(4-OCHF₂) A-0774 CH₂CF₃ Me F 1 CH₂CH₂Ph(4-OCHF₂) A-0775 CH₂CF₃ Me Me 1 CH₂CH₂Ph(4-OCHF₂) A-0776 CH₂CF₃ Cl Cl 1 CH₂CH₂Ph(4-OCHF₂) A-0777 CH₂CF₃ Me F 0 CH₂Ph(3-OCF₃) A-0778 CH₂CF₃ Me F 0 CH₂CH₂Ph(4-OCF₃) A-0779 CH₂CF₃ Me F 1 CH₂CH₂Ph(4-OCF₃) A-0780 CH₂CF₃ Cl F 0 CH₂CH₂Ph(4-OCF₃) A-0781 CH₂CF₃ Cl F 1 CH₂CH₂Ph(4-OCF₃) A-0782 CH₂CF₃ Cl Cl 1 CH₂CH₂Ph(4-OCF₃) A-0783 CH₂CF₃ Me Me 1 CH₂CH₂Ph(4-OCF₃) A-0784 CH₂CF₃ Me Cl 1 CH₂CH₂Ph(4-OCF₃) A-0785 CH₂CF₃ Me F 0 CH₂CH₂Ph(4-SCHF₂) A-0786 CH₂CF₃ Me F 0 CH₂CH₂Ph(4-SCF₃) A-0787 CH₂CF₃ Cl F 0 CH₂CH₂Ph(4-SCF₃) A-0788 CH₂CF₃ Me F 1 CH₂CH₂Ph(4-SCF₃) A-0789 CH₂CF₃ Cl F 1 CH₂CH₂Ph(4-SCF₃) A-0790 CH₂CF₃ Cl Cl 0 CH₂CH₂Ph(4-SCF₃)

TABLE 21 Compound No. R¹ R² R³ n R⁴ A-0791 CH₂CF₃ Cl Cl 1 CH₂CH₂Ph(4-SCF₃) A-0792 CH₂CF₃ Me Me 1 CH₂CH₂Ph(4-SCF₃) A-0793 CH₂CF₃ Me Cl 1 CH₂CH₂Ph(4-SCF₃) A-0794 CH₂CF₃ Me F 1 CH₂CH₂Ph(4-CF(CF₃)₂) A-0795 CH₂CF₃ Me F 0 CH₂CH₂Ph(4-NO₂) A-0796 CH₂CF₃ Me F 1 CH₂CH₂Ph(4-NO₂) A-0797 CH₂CF₃ Cl F 0 CH₂CH₂Ph(4-OS(═O)₂CF₃) A-0798 CH₂CF₃ Me F 0 CH₂CH₂Ph(4-OS(═O)₂CF₃) A-0799 CH₂CF₃ Me F 1 CH₂CH₂Ph(4-OS(═O)₂CF₃) A-0800 CH₂CF₃ Cl F 1 CH₂CH₂Ph(4-OS(═O)₂CF₃) A-0801 CH₂CF₃ Me F 1 CH₂CH₂Ph(2,4-Cl₂) A-0802 CH₂CF₃ Me F 0 CH₂CH₂Ph(3,4-Cl₂) A-0803 CH₂CF₃ Me F 1 CH₂CH₂Ph(3,4-Cl₂) A-0804 CH₂CF₃ Me F 1 CH₂CH₂Ph(3,4,5-Cl₃) A-0805 CH₂CF₃ Me F 1 CH₂CH₂Ph(2,3,4-F₃) A-0806 CH₂CF₃ Cl F 1 CH₂CH₂Ph(2,3,4-F₃) A-0807 CH₂CF₃ Me F 1 CH₂CH₂Ph(2,4,5-F₃) A-0808 CH₂CF₃ Cl F 1 CH₂CH₂Ph(2,4,5-F₃) A-0809 CH₂CF₃ Me F 0 CH₂CH₂Ph(3,4,5-F₃) A-0810 CH₂CF₃ Me F 1 CH₂CH₂Ph(3,4,5-F₃) A-0811 CH₂CF₃ Me F 0 CH₂CH₂Ph(2,4,6-F₃) A-0812 CH₂CF₃ Me F 1 CH₂CH₂Ph(2,4,6-F₃) A-0813 CH₂CF₃ Me F 0 CH₂CH₂Ph(3-CF₃, 4-F) A-0814 CH₂CF₃ Me F 1 CH₂CH₂Ph(3-CF₃, 4-F) A-0815 CH₂CF₃ Cl F 0 CH₂CH₂Ph(3-CF₃, 4-F) A-0816 CH₂CF₃ Cl F 1 CH₂CH₂Ph(3-CF₃, 4-F) A-0817 CH₂CF₃ Cl F 1 CH₂CH₂Ph(2-F, 4-CF₃) A-0818 CH₂CF₃ Me Cl 1 CH₂CH₂Ph(2-F, 4-CF₃) A-0819 CH₂CF₃ Cl Cl 0 CH₂CH₂Ph(2-F, 4-CF₃) A-0820 CH₂CF₃ Cl Cl 1 CH₂CH₂Ph(2-F, 4-CF₃) A-0821 CH₂CF₃ Me F 1 CH₂CH₂Ph(3-F, 4-CF₃) A-0822 CH₂CF₃ Me F 0 CH₂CH₂Ph(3-F, 4-CF₃) A-0823 CH₂CF₃ Cl F 1 CH₂CH₂Ph(3-F, 4-CF₃) A-0824 CH₂CF₃ Cl F 0 CH₂CH₂Ph(3-F, 4-CF₃) A-0825 CH₂CF₃ Me F 1 CH₂CH₂Ph(2-F, 4-CF₃) A-0826 CH₂CF₃ Cl F 0 CH₂CH₂Ph(3-Cl, 4-OCHF₂) A-0827 CH₂CF₃ Cl F 1 CH₂CH₂Ph(3-Cl, 4-OCHF₂) A-0828 CH₂CF₃ Me F 0 CH₂CH₂Ph(4-Ph(4-CF₃)) A-0829 CH₂CF₃ Me F 1 CH₂CH₂Ph(4-Ph(4-CF₃)) A-0830 CH₂CF₃ Me F 0 CH₂CH₂Ph(4-OCH₂Ph)

TABLE 22 Compound No. R¹ R² R³ n R⁴ A-0831 CH₂CF₃ Me F 1 CH₂CH₂Ph(4-OCH₂Ph) A-0832 CH₂CF₃ Cl F 0 CH₂C(Me)₂Ph(4-Cl) A-0833 CH₂CF₃ Cl F 1 CH₂C(Me)₂Ph(4-Cl) A-0834 CH₂CF₃ Me F 0 CH₂CH₂CH₂Ph A-0835 CH₂CF₃ Me F 0 CH₂CH(CH₃)Ph A-0836 CH₂CF₃ Me F 0 CH(CH₃)CH₂Ph A-0837 CH₂CF₃ Me F 1 CH₂CH₂CH₂Ph A-0838 CH₂CF₃ Me F 0 CH₂CH₂CH₂Ph(4-CF₃) A-0839 CH₂CF₃ Me F 1 CH₂CH₂CH₂Ph(4-CF₃) A-0840 CH₂CF₃ Cl F 1 CH₂CH₂CH₂Ph(4-CF₃) A-0841 CH₂CF₃ Me Cl 1 CH₂CH₂CH₂Ph(4-CF₃) A-0842 CH₂CF₃ Cl Cl 1 CH₂CH₂CH₂Ph(4-CF₃) A-0843 CH₂CF₃ Me Me 1 CH₂CH₂CH₂Ph(4-CF₃) A-0844 CH₂CF₃ Me F 0 CH₂CH₂CH₂Ph(3-CF₃) A-0845 CH₂CF₃ Me F 1 CH₂CH₂CH₂Ph(3-CF₃) A-0846 CH₂CF₃ Me F 0 CH₂CH₂CH₂Ph(4-tBu) A-0847 CH₂CF₃ Me F 1 CH₂CH₂CH₂Ph(4-tBu) A-0848 CH₂CF₃ Me F 0 CH₂CH₂CH₂Ph(4-CN) A-0849 CH₂CF₃ Me F 1 CH₂CH₂CH₂Ph(4-CN) A-0850 CH₂CF₃ Me F 1 CH₂CH₂CH₂Ph(4-OCHF₂) A-0851 CH₂CF₃ Me F 1 CH₂CH₂CH₂Ph(4-OCF₃) A-0852 CH₂CF₃ Me F 1 CH₂CH₂CH₂Ph(4-SCHF₂) A-0853 CH₂CF₃ Me F 0 CH₂CH₂CH₂Ph(4-SCF₃) A-0854 CH₂CF₃ Me F 1 CH₂CH₂CH₂Ph(4-SCF₃) A-0855 CH₂CF₃ Me F 0 CH₂CH₂CH₂Ph(3,4,5-F₃) A-0856 CH₂CF₃ Me F 1 CH₂CH₂CH₂Ph(3,4,5-F₃) A-0857 CH₂CF₃ Me F 0 CH₂CH₂CH₂Ph(2,4,6-F₃) A-0858 CH₂CF₃ Me F 1 CH₂CH₂CH₂Ph(2,4,6-F₃) A-0859 CH₂CF₃ Me F 1 CH₂CH₂CH₂Ph(4-CF(CF₃)₂) A-0860 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂Ph A-0861 CH₂CF₃ Me F 0 CH₂CH₂CH(CH₃)Ph A-0862 CH₂CF₃ Me F 0 CH₂CH(CH₃)CH₂Ph A-0863 CH₂CF₃ Me F 0 CH(CH₃)CH₂CH₂Ph A-0864 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂Ph A-0865 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂Ph(4-F) A-0866 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂Ph(4-CF₃) A-0867 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂Ph(4-OCF₃) A-0868 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂Ph(4-SCF₃) A-0869 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂CH₂Ph A-0870 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂CH₂CH₂Ph

TABLE 23 Compound No. R¹ R² R³ n R⁴ A-0871 CH₂CF₃ Me F 0 CH₂CH₂SPh A-0872 CH₂CF₃ Me F 0 CH₂CH₂CH₂SPh A-0873 CH₂CF₃ Me F 1 CH₂CH₂CH₂SPh A-0874 CH₂CF₃ Me F 0 CH₂CH(CH₃)SPh A-0875 CH₂CF₃ Me F 0 CH(CH₃)CH₂SPh A-0876 CH₂CF₃ Me F 1 CH₂CH₂CH₂SPh(4-Cl) A-0877 CH₂CF₃ Me F 1 CH₂CH₂CH₂SPh(4-tBu) A-0878 CH₂CF₃ Me F 1 CH₂CH₂CH₂SPh(4-F) A-0879 CH₂CF₃ Me F 0 CH₂CH₂CH₂SPh(4-Br) A-0880 CH₂CF₃ Me F 0 CH₂CH₂CH₂SPh(4-CF₃) A-0881 CH₂CF₃ Me F 1 CH₂CH₂CH₂SPh(4-CF₃) A-0882 CH₂CF₃ Cl F 0 CH₂CH₂CH₂SPh(4-CF₃) A-0883 CH₂CF₃ Me H 0 CH₂CH₂CH₂SPh(4-CF₃) A-0884 CH₂CF₃ Me F 0 CH₂CH₂CH₂SPh(3-CF₃) A-0885 CH₂CF₃ Me F 1 CH₂CH₂CH₂SPh(3-CF₃) A-0886 CH₂CF₃ Me F 1 CH₂CH₂CH₂SPh(3-SCF₃) A-0887 CH₂CF₃ Me F 1 CH₂CH₂CH₂SPh(4-SCF₃) A-0888 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂SPh A-0889 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂SPh(4-Cl) A-0890 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂SPh(4-F) A-0891 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂SPh(4-tBu) A-0892 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂SPh(3-CF₃) A-0893 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂CH₂SPh A-0894 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂CH₂SPh(4-CF₃) A-0895 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂CH₂SPh(4-Cl) A-0896 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂CH₂SPh(4-F) A-0897 CH₂CF₃ Me F 0 CH₂CH₂S(═O)Ph A-0898 CH₂CF₃ Me F 0 CH₂CH₂CH₂S(═O)Ph A-0899 CH₂CF₃ Me F 1 CH₂CH₂CH₂S(═O)Ph A-0900 CH₂CF₃ Me F 0 CH₂CH₂CH₂S(═O)Ph(4-CF₃) A-0901 CH₂CF₃ Me F 1 CH₂CH₂CH₂S(═O)Ph(4-CF₃) A-0902 CH₂CF₃ Me F 1 CH₂CH₂CH₂S(═O)Ph(4-F) A-0903 CH₂CF₃ Me F 1 CH₂CH₂CH₂S(═O)Ph(4-tBu) A-0904 CH₂CF₃ Me F 1 CH₂CH₂CH₂S(═O)₂Ph(4-CF₃) A-0905 CH₂CF₃ Me F 1 CH₂CH₂CH₂S(═O)₂Ph(4-Cl) A-0906 CH₂CF₃ Me F 1 CH₂CH₂CH₂S(═O)₂Ph(4-F) A-0907 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂S(═O)₂Ph A-0908 CH₂CF₃ Cl F 0 CH₂CH₂CH₂CH₂S(═O)₂Ph A-0909 CH₂CF₃ Cl F 1 CH₂CH₂CH₂CH₂S(═O)₂Ph A-0910 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂S(═O)₂Ph(4-CF₃)

TABLE 24 Compound No. R¹ R² R³ n R⁴ A-0911 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂S(═O)₂Ph(4-Cl) A-0912 CH₂CF₃ Me F 0 CH₂CH₂SCH₂Ph A-0913 CH₂CF₃ Me F 0 CH₂CH₂CH₂SCH₂Ph A-0914 CH₂CF₃ Cl F 0 CH₂CH₂CH₂SCH₂Ph A-0915 CH₂CF₃ Me Cl 0 CH₂CH₂CH₂SCH₂Ph A-0916 CH₂CF₃ CN F 0 CH₂CH₂CH₂SCH₂Ph A-0917 CH₂CF₃ Me H 0 CH₂CH₂CH₂SCH₂Ph A-0918 CH₂CF₃ Me F 1 CH₂CH₂CH₂SCH₂Ph A-0919 CH₂CF₃ Me F 0 CH₂CH₂CH₂SCH₂Ph(2-Cl) A-0920 CH₂CF₃ Me F 0 CH₂CH₂CH₂SCH₂Ph(3-Cl) A-0921 CH₂CF₃ Me F 0 CH₂CH₂CH₂SCH₂Ph(4-Cl) A-0922 CH₂CF₃ Me F 1 CH₂CH₂CH₂SCH₂Ph(4-Cl) A-0923 CH₂CF₃ Me F 0 CH₂CH₂CH₂SCH₂Ph(4-CF₃) A-0924 CH₂CF₃ Me F 1 CH₂CH₂CH₂SCH₂Ph(4-CF₃) A-0925 CH₂CF₃ Me F 1 CH₂CH₂CH₂SCH₂Ph(3-CF₃) A-0926 CH₂CF₃ Me F 0 CH₂CH₂CH₂SCH₂Ph(4-NO₂) A-0927 CH₂CF₃ Me F 1 CH₂CH₂CH₂SCH₂Ph(2-SCF₃) A-0928 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂SCH₂Ph A-0929 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂SCH₂Ph(4-CF₃) A-0930 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂SCH₂Ph(4-Cl) A-0931 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂SCH₂Ph(4-CN) A-0932 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂CH₂SCH₂Ph A-0933 CH₂CF₃ Me F 0 CH₂CH₂SCH₂CH₂Ph A-0934 CH₂CF₃ Me F 0 CH₂CH₂SCH(Me)Ph A-0935 CH₂CF₃ Me F 0 CH₂CH₂CH₂SCH₂CH₂Ph A-0936 CH₂CF₃ Me F 0 CH₂CH₂CH₂SCH(Me)Ph A-0937 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂SCH₂CH₂Ph A-0938 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂SCH(Me)Ph A-0939 CH₂CF₃ Me F 0 CH₂CH₂S(═O)CH₂Ph(4-CF₃) A-0940 CH₂CF₃ Me F 0 CH₂CH₂CH₂S(═O)CH₂Ph A-0941 CH₂CF₃ Me F 0 CH₂CH₂CH₂S(═O)CH₂Ph(4-CF₃) A-0942 CH₂CF₃ Me F 1 CH₂CH₂CH₂S(═O)CH₂Ph(4-Cl) A-0943 CH₂CF₃ Me F 1 CH₂CH₂CH₂S(═O) CH₂Ph(2-SCF₃) A-0944 CH₂CF₃ Me F 0 CH₂CH₂CH₂S(═O) CH₂Ph(4-SCF₃) A-0945 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂S(═O)CH₂Ph(4-CF₃) A-0946 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂CH₂S(═O)CH₂Ph(4-CF₃) A-0947 CH₂CF₃ Me F 0 CH₂CH₂S(═O)₂CH₂Ph(4-CF₃) A-0948 CH₂CF₃ Me F 0 CH₂CH₂CH₂S(═O)₂CH₂Ph A-0949 CH₂CF₃ Me F 0 CH₂CH₂CH₂S(═O)₂CH₂Ph(4-CF₃) A-0950 CH₂CF₃ Me F 1 CH₂CH₂CH₂S(═O)₂CH₂Ph(4-Cl)

TABLE 25 Compound No. R¹ R² R³ n R⁴ A-0951 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂S(═O)₂CH₂Ph(4-CF₃) A-0952 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂CH₂S(═O)₂CH₂Ph(4-CF₃) A-0953 CH₂CF₃ Me F 0 CH₂CH₂OPh(4-CF₃) A-0954 CH₂CF₃ Me F 0 CH₂CH₂CH₂OPh A-0955 CH₂CF₃ Me F 0 CH₂CH₂CH₂OPh(4-Cl) A-0956 CH₂CF₃ Cl F 0 CH₂CH₂CH₂OPh(4-CF₃) A-0957 CH₂CF₃ Cl F 1 CH₂CH₂CH₂OPh(4-CF₃) A-0958 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂OPh(4-CF₃) A-0959 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂OPh(4-OCF₃) A-0960 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂OPh(4-OCF₃) A-0961 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂CH₂OPh(4-CF₃) A-0962 CH₂CF₃ Me H 0 CH₂CH₂OCH₂Ph A-0963 CH₂CF₃ Me H 0 CH₂CH₂CH₂OCH₂Ph A-0964 CH₂CF₃ Me H 1 CH₂CH₂CH₂OCH₂Ph A-0965 CH₂CF₃ Me F 0 CH₂CH₂CH₂OCH₂Ph A-0966 CH₂CF₃ Me F 1 CH₂CH₂CH₂OCH₂Ph A-0967 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂OCH₂Ph A-0968 CH₂CF₃ Me F 0 CH₂CH₂ON═C(Me)CF₃ A-0969 CH₂CF₃ Me F 1 CH₂CH₂ON═C(Me)CF₃ A-0970 CH₂CF₃ Me F 0 CH₂CH₂CH₂ON═CHtBu A-0971 CH₂CF₃ Me F 1 CH₂CH₂CH₂ON═CHtBu A-0972 CH₂CF₃ Me F 0 CH₂CH₂CH₂ON═C(Me)CF₃ A-0973 CH₂CF₃ Me F 1 CH₂CH₂CH₂ON═C(Me)CF₃ A-0974 CH₂CF₃ Me F 1 CH₂CH(CH₃)ON═C(Me)CF₃ A-0975 CH₂CF₃ Me F 0 CH₂CH₂CH₂ON═CHCF₃ A-0976 CH₂CF₃ Me F 1 CH₂CH₂CH₂ON═CHCF₃ A-0977 CH₂CF₃ Cl F 0 CH₂CH₂CH₂ON═C(Me)CF₃ A-0978 CH₂CF₃ Cl F 1 CH₂CH₂CH₂ON═C(Me)CF₃ A-0979 CH₂CF₃ Me F 0 CH₂CH₂CH₂ON═C(Me)CCl₃ A-0980 CH₂CF₃ Me F 1 CH₂CH₂CH₂ON═C(Me)CCl₃ A-0981 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂ON═CHCF₃ A-0982 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂ON═CHCF₃ A-0983 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂ON═C(Me)CF₃ A-0984 CH₂CF₃ Cl F 0 CH₂CH₂CH₂CH₂ON═C(Me)CF₃ A-0985 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂ON═C(Me)CF₃ A-0986 CH₂CF₃ Me F 1 CH₂CH₂CH(CH₃)ON═C(Me)CF₃ A-0987 CH₂CF₃ Me F 1 CH₂CH(CH₃)CH₂ON═C(Me)CF₃ A-0988 CH₂CF₃ Cl F 1 CH₂CH₂CH₂CH₂ON═C(Me)CF₃ A-0989 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂ON═C(Me)cPr A-0990 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂ON═C(Me)cPr

TABLE 26 Compound No. R¹ R² R³ n R⁴ A-0991 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂CH₂ON═C(Me)CF₃ A-0992 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂ON═C(Me)CF₃ A-0993 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH(CH₃)ON═C(Me)CF₃ A-0994 CH₂CF₃ Me F 1 CH₂CH₂CH(CH₃)CH₂ON═C(Me)CF₃ A-0995 CH₂CF₃ Me F 1 CH₂CH(CH₃)CH₂CH₂ON═C(Me)CF₃ A-0996 CH₂CF₃ Me F 0

A-0997 CH₂CF₃ Me F 1

A-0998 CH₂CF₃ Me F 0 CH₂CH₂ON═CHPh A-0999 CH₂CF₃ Me F 0 CH₂CH₂ON═CHPh(4-CF₃) A-1000 CH₂CF₃ Me F 1 CH₂CH₂ON═CHPh(4-CF₃) A-1001 CH₂CF₃ Me F 0 CH₂CH₂ON═CHPh(4-SCF₃) A-1002 CH₂CF₃ Me F 1 CH₂CH₂ON═CHPh(4-SCF₃) A-1003 CH₂CF₃ Me F 0 CH₂CH₂CH₂ON═CHPh(4-CF₃) A-1004 CH₂CF₃ Me F 0 CH₂CH₂CH₂ON═CHPh(3-CF₃) A-1005 CH₂CF₃ Me F 1 CH₂CH₂CH₂ON═CHPh(4-CF₃) A-1006 CH₂CF₃ Me F 1 CH₂CH₂CH₂ON═CHPh(3-CF₃) A-1007 CH₂CF₃ Me F 0 CH₂CH₂CH₂ON═CHPh(4-SCF₃) A-1008 CH₂CF₃ Me F 1 CH₂CH₂CH₂ON═CHPh(4-SCF₃) A-1009 CH₂CF₃ Me F 0 CH₂CH₂CH₂ON═C(Me)Ph(4-CF₃) A-1010 CH₂CF₃ Me F 1 CH₂CH₂CH₂ON═C(Me)Ph(4-CF₃) A-1011 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂ON═CHPh(4-SCF₃) A-1012 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂ON═CHPh(4-SCF₃) A-1013 CH₂CF₃ Me F 1 CH₂CH₂SC(═O)NMe₂ A-1014 CH₂CF₃ Me F 1 CH₂CH₂SC(═O)NHCH₂CF₃ A-1015 CH₂CF₃ Me F 0 CH₂CH₂CH₂SC(═O)NMe₂ A-1016 CH₂CF₃ Me F 1 CH₂CH₂CH₂SC(═O)NMe₂ A-1017 CH₂CF₃ Me F 1 CH₂CH₂CH₂SC(═O)NHtBu A-1018 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂SC(═O)NHCH₂CF₃ A-1019 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂SC(═O)NHtBu A-1020 CH₂CF₃ Cl F 0 CH₂CH₂CH₂NHC(═O)OtBu A-1021 CH₂CF₃ Cl F 1 CH₂CH₂CH₂NHC(═O)OtBu A-1022 CH₂CF₃ Me F 1 CH₂CH₂CH₂NHC(═O)OCH₂CF₃ A-1023 CH₂CF₃ Me F 1 CH₂CH₂CH₂NHC(═O)OCH₂CH₂CF₃ A-1024 CH₂CF₃ Cl F 0 CH₂CH₂CH₂CH₂CH₂OC(═O)Me A-1025 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂CH₂OC(═O)Me A-1026 CH₂CF₃ Me H 0 CH₂CH₂OC(═O)Ph A-1027 CH₂CF₃ Me H 1 CH₂CH₂OC(═O)Ph A-1028 CH₂CF₃ Me F 0 CH₂CH₂OC(═O)Ph(4-CF₃)

TABLE 27 Compound No. R¹ R² R³ n R⁴ A-1029 CH₂CF₃ Me F 0 CH₂CH₂CH₂OC(═O)Ph(4-CF₃) A-1030 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂OC(═O)Ph(4-CF₃) A-1031 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂CH₂OC(═O)Ph(4-CF₃) A-1032 CH₂CF₃ Me F 0 CH₂CH₂OS(═O)₂Me A-1033 CH₂CF₃ Me F 0 CH₂CH₂CH₂OS(═O)₂Me A-1034 CH₂CF₃ Me F 1 CH₂CH₂CH₂OS(═O)₂CF₃ A-1035 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂OS(═O)₂CF₃ A-1036 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂OS(═O)₂CF₃ A-1037 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂CH₂OS(═O)₂CF₂CF₂CF₂CF₃ A-1038 CH₂CF₃ Me F 1 CH₂CH₂OS(═O)CF₃ A-1039 CH₂CF₃ Me F 1 CH₂CH₂CH₂OS(═O)CF₃ A-1040 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂OS(═O)CF₃ A-1041 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂OS(═O)CF₃ A-1042 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂CH₂CH₂OS(═O)CF₃ A-1043 CH₂CF₃ Me F 0 CH₂CH₂ONH₂ A-1044 CH₂CF₃ Me F 0 CH₂CH₂CH₂ONH₂ A-1045 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂ONH₂ A-1046 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂CH₂ONH₂ A-1047 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂CH₂CH₂ONH₂ A-1048 CH₂CF₃ Me F 0 CH₂C(═O)OEt A-1049 CH₂CF₃ Me F 1 CH₂CH₂C(═O)OtBu A-1050 CH₂CF₃ Me F 0 CH₂CH₂CH₂C(═O)OEt A-1051 CH₂CF₃ Me F 0 CH₂CH₂CH₂C(═O)OtBu A-1052 CH₂CF₃ Me F 1 CH₂CH₂CH₂C(═O)OtBu A-1053 CH₂CF₃ Me F 1 CH₂CH₂CH₂C(═O)OtBu A-1054 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂C(═O)OtBu A-1055 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂C(═O)OtBu A-1056 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂CH₂C(═O)OtBu A-1057 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂CH₂CH₂CH₂C(═O)OEt A-1058 CH₂CF₃ Cl F 0 CH₂CH₂CH₂CH₂CH₂CH₂CH₂C(═O)OEt A-1059 CH₂CF₃ Cl F 0 CH₂CH₂CH₂CH₂C(═O)OH A-1060 CH₂CF₃ Cl Cl 0 CH₂CH₂CH₂CH₂C(═O)OH A-1061 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂CH₂CH₂CH₂C(═O)OH A-1062 CH₂CF₃ Me F 0 CH₂CH₂CH₂C(═O)NH(tert-pentyl) A-1063 CH₂CF₃ Me F 0 CH₂CH₂C(═O)NHtBu A-1064 CH₂CF₃ Me F 0 CH₂CH₂C(═O)NHCH₂CF₃ A-1065 CH₂CF₃ Me F 0 CH₂CH₂CH₂C(═O)NHtBu A-1066 CH₂CF₃ Me F 0 CH₂CH₂CH₂C(═O)NHCH₂CF₃ A-1067 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂C(═O)NHtBu A-1068 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂C(═O)NHCH₂CF₃

TABLE 28 Compound No. R¹ R² R³ n R⁴ A-1069 CH₂CF₃ Me F 1 CH₂CH₂CH₂C(═O)CF₃ A-1070 CH₂CF₃ Cl F 1 CH₂CH₂CH₂C(═O)CF₃ A-1071 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂C(═O)CF₃ A-1072 CH₂CF₃ Cl F 0 CH₂CH₂CH₂CH₂C(═O)CF₃ A-1073 CH₂CF₃ Cl F 1 CH₂CH₂CH₂CH₂C(═O)CF₃ A-1074 CH₂CF₃ Cl Cl 0 CH₂CH₂CH₂CH₂C(═O)CF₃ A-1075 CH₂CF₃ Cl Cl 1 CH₂CH₂CH₂CH₂C(═O)CF₃ A-1076 CH₂CF₃ Me Me 1 CH₂CH₂CH₂CH₂C(═O)CF₃ A-1077 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂C(═O)CF₃ A-1078 CH₂CF₃ Cl F 1 CH₂CH₂CH₂CH₂CH₂C(═O)CF₃ A-1079 CH₂CF₃ Me F 0 CH₂C(═O)Ph(4-Cl) A-1080 CH₂CF₃ Me F 1 CH₂C(═O)Ph(4-Cl) A-1081 CH₂CF₃ Me F 0 CH₂C(═O)Ph(4-CF₃) A-1082 CH₂CF₃ Me F 1 CH₂C(═O)Ph(4-CF₃) A-1083 CH₂CF₃ Me F 0 CH₂CH₂C(═O)Ph(4-CF₃) A-1084 CH₂CF₃ Me F 0 CH₂CH₂CH₂C(═O)Ph(4-CF₃) A-1085 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂C(═O)Ph(4-CF₃) A-1086 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂CH₂C(═O)Ph(4-CF₃) A-1087 CH₂CF₃ Me F 0 CH₂CH₂CH₂CN A-1088 CH₂CF₃ Me F 1 CH₂CH₂CH₂CN A-1089 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CN A-1090 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂CN A-1091 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂CH₂CN A-1092 CH₂CF₃ Me F 1 cPr A-1093 CH₂CF₃ Me F 0 cPen A-1094 CH₂CF₃ Me F 1 cPen A-1095 CH₂CF₃ Me F 0 cHex A-1096 CH₂CF₃ Me F 1 cHex A-1097 CH₂CF₃ CN F 0 cHex A-1098 CH₂CF₃ CN F 1 cHex A-1099 CH₂CF₃ Me F 0 CH₂CH₂NH₂ A-1100 CH₂CF₃ Cl F 0 CH₂CH₂CH₂NH₂ A-1101 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂NH₂ A-1102 CH₂CF₃ Cl F 1 CH₂CH₂CH₂CH₂NH₂ A-1103 CH₂CF₃ Me F 1 CH₂CH₂CH₂N(Me)tBu A-1104 CH₂CF₃ Me F 1 CH₂CH₂CH₂NHCH₂CF₃ A-1105 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂N(Me)tBu A-1106 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂NHCH₂CF₃ A-1107 CH₂CF₃ Cl F 0 CH₂CH₂NHC(═O)C(Me)(CF₃)₂ A-1108 CH₂CF₃ Cl F 1 CH₂CH₂NHC(═O)C(Me)(CF₃)₂

TABLE 29 Compound No. R¹ R² R³ n R⁴ A-1109 CH₂CF₃ Me F 1 CH₂CH₂CH₂N(Me)C(═O)tBu A-1110 CH₂CF₃ Me F 1 CH₂CH₂CH₂NHC(═O)CH₂CF₃ A-1111 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂NHC(═O)CH(CH₃)₂ A-1112 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂NHC(═O)tBu A-1113 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂NHC(═O)tBu A-1114 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂NHC(═O)CH₂tBu A-1115 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂N(Me)C(═O)tBu A-1116 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂NHC(═O)CF₃ A-1117 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂NHC(═O)CF₃ A-1118 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂NHC(═O)CH₂CF₃ A-1119 CH₂CF₃ Cl F 1 CH₂CH₂CH₂CH₂NHC(═O)CH₂CF₃ A-1120 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂NHC(═O)CCl₃ A-1121 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂NHC(═O)CF(CF₃)₂ A-1122 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂NHC(═O)Ph A-1123 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂NHC(═O)Ph A-1124 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂NHC(═O)OCH(CH₃)₂ A-1125 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂NHC(═O)OtBu A-1126 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂NHC(═O)OtBu A-1127 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂NHC(═O)OCH₂CCl₃ A-1128 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂NHC(═O)OCH₂CCl₃ A-1129 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂NHC(═O)OCH₂CF₃ A-1130 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂NHC(═O)NHEt A-1131 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂NHC(═O)NHtBu A-1132 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂NHC(═O)NHtBu A-1133 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂NHC(═O)NHCH₂CCl₃ A-1134 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂NHC(═O)NHCH₂CH₂F A-1135 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂NHC(═O)NHCH₂CF₃ A-1136 CH₂CF₃ Me F 0 CH₂CH₂NHS(═O)₂CF₃ A-1137 CH₂CF₃ Me F 1 CH₂CH₂NHS(═O)₂CF₃ A-1138 CH₂CF₃ Cl F 0 CH₂CH₂NHS(═O)₂CF₃ A-1139 CH₂CF₃ Cl F 1 CH₂CH₂NHS(═O)₂CF₃ A-1140 CH₂CF₃ Me F 0 CH₂CH₂CH₂NHS(═O)₂CF₃ A-1141 CH₂CF₃ Me F 1 CH₂CH₂CH₂NHS(═O)₂CF₃ A-1142 CH₂CF₃ Cl F 0 CH₂CH₂CH₂NHS(═O)₂CF₃ A-1143 CH₂CF₃ Cl F 1 CH₂CH₂CH₂NHS(═O)₂CF₃ A-1144 CH₂CF₃ Me Cl 1 CH₂CH₂CH₂NHS(═O)₂CF₃ A-1145 CH₂CF₃ CN F 1 CH₂CH₂CH₂NHS(═O)₂CF₃ A-1146 CH₂CF₃ CN F 1 CH₂CH₂CH₂NHS(═O)₂CHF₂ A-1147 CH₂CF₃ Me F 1 CH₂CH₂CH₂NHS(═O)₂CF(CF₃)₂ A-1148 CH₂CF₃ Cl F 1 CH₂CH₂CH₂NHS(═O)₂CF(CF₃)₂

TABLE 30 Compound No. R¹ R² R³ n R⁴ A-1149 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂NHS(═O)₂CH₃ A-1150 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂NHS(═O)₂CH₃ A-1151 CH₂CF₃ Cl F 0 CH₂CH₂CH₂CH₂NHS(═O)₂CH₃ A-1152 CH₂CF₃ Cl F 1 CH₂CH₂CH₂CH₂NHS(═O)₂CH₃ A-1153 CH₂CF₃ Cl F 1 CH₂CH₂CH₂CH₂NHS(═O)₂CH(CH₃)₂ A-1154 CH₂CF₃ Cl F 1 CH₂CH₂CH₂CH₂NHS(═O)₂CHF₂ A-1155 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂NHS(═O)₂CHF₂ A-1156 CH₂CF₃ Cl F 0 CH₂CH₂CH₂CH₂NHS(═O)₂CF₃ A-1157 CH₂CF₃ Cl F 1 CH₂CH₂CH₂CH₂NHS(═O)₂CF₃ A-1158 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂NHS(═O)₂CF₃ A-1159 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂NHS(═O)₂CF₃ A-1160 CH₂CF₃ Me Cl 1 CH₂CH₂CH₂CH₂NHS(═O)₂CF₃ A-1161 CH₂CF₃ Me H 1 CH₂CH₂CH₂CH₂NHS(═O)₂CF₃ A-1162 CH₂CF₃ Cl Cl 1 CH₂CH₂CH₂CH₂NHS(═O)₂CF₃ A-1163 CH₂CF₃ Me Me 1 CH₂CH₂CH₂CH₂NHS(═O)₂CF₃ A-1164 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂CH₂NHS(═O)₂CH₃ A-1165 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂NHS(═O)₂CH₃ A-1166 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂NHS(═O)₂CHF₂ A-1167 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂NHS(═O)₂CF₃ A-1168 CH₂CF₃ Cl F 1 CH₂CH₂CH₂CH₂CH₂NHS(═O)₂CF₃ A-1169 CH₂CF₃ Me Cl 1 CH₂CH₂CH₂CH₂CH₂NHS(═O)₂CF₃ A-1170 CH₂CF₃ Cl Cl 1 CH₂CH₂CH₂CH₂CH₂NHS(═O)₂CF₃ A-1171 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂CH₂NHS(═O)₂Ph A-1172 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂NHS(═O)₂Ph A-1173 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂CH₂NHS(═O)₂Ph(4-CF₃) A-1174 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂NHS(═O)₂Ph(4-CF₃) A-1175 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂CH₂NHS(═O)₂CF₃ A-1176 CH₂CF₃ Me F 1 CH₂CH₂N(Me)S(═O)₂CF₃ A-1177 CH₂CF₃ Me F 0 CH₂CH₂N(Ac)S(═O)₂CF₃ A-1178 CH₂CF₃ Me F 1 CH₂CH₂N(Ac)S(═O)₂CF₃ A-1179 CH₂CF₃ Me F 1 CH₂CH₂N(COtBu)S(═O)₂CF₃ A-1180 CH₂CF₃ Me F 0 CH₂CH₂N(CO₂CH₃)S(═O)₂CF₃ A-1181 CH₂CF₃ Me F 1 CH₂CH₂N(CO₂CH₃)S(═O)₂CF₃ A-1182 CH₂CF₃ Cl F 0 CH₂CH₂N(CO₂CH₃)S(═O)₂CF₃ A-1183 CH₂CF₃ Cl F 1 CH₂CH₂N(CO₂CH₃)S(═O)₂CF₃ A-1184 CH₂CF₃ Me F 1 CH₂CH₂CH₂N(Me)S(═O)₂CF₃ A-1185 CH₂CF₃ Me F 0 CH₂CH₂CH₂N(Ac)S(═O)₂CF₃ A-1186 CH₂CF₃ Me F 1 CH₂CH₂CH₂N(Ac)S(═O)₂CF₃ A-1187 CH₂CF₃ Cl F 1 CH₂CH₂CH₂N(CO₂CH₃)S(═O)₂CF₃ A-1188 CH₂CF₃ Me F 1 CH₂CH₂CH₂N(CO₂CH₃)S(═O)₂CF₃

TABLE 31 Compound No. R¹ R² R³ n R⁴ A-1189 CH₂CF₃ Me F 1 CH₂CH₂CH₂N(CO₂tBu)S(═O)₂CF₃ A-1190 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂N(Me)S(═O)₂CF₃ A-1191 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂N(Ac)S(═O)₂CF₃ A-1192 CH₂CF₃ Cl F 1 CH₂CH₂CH₂CH₂N(Ac)S(═O)₂CF₃ A-1193 CH₂CF₃ Cl F 1 CH₂CH₂CH₂CH₂N(propionyl)S(═O)₂CF₃ A-1194 CH₂CF₃ Cl F 1 CH₂CH₂CH₂CH₂N(pivaloyl)S(═O)₂CF₃ A-1195 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂N(CO₂CH₃)S(═O)₂CF₃ A-1196 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂N(CO₂CH₃)S(═O)₂CF₃ A-1197 CH₂CF₃ Cl F 1 CH₂CH₂CH₂CH₂N(CO₂CH₃)S(═O)₂CF₃ A-1198 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂N(CO₂tBu)S(═O)₂CF₃ A-1199 CH₂CF₃ Cl F 1 CH₂CH₂CH₂CH₂N(CO₂tBu)S(═O)₂CF₃ A-1200 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂N(Ac)S(═O)₂CF₃ A-1201 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂CH₂N(CO₂CH₃)S(═O)₂CF₃ A-1202 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂CH₂N(CO₂CH₃)S(═O)₂CF₃ A-1203 CH₂CF₃ Me F 1 CH₂CH₂SiMe₃ A-1204 CH₂CF₃ Cl F 1 CH₂CH₂SiMe₃ A-1205 CH₂CF₃ Me F 0 CH₂CH₂CH₂SiMe₃ A-1206 CH₂CF₃ Me H 0 CH₂CH₂CH₂SiMe₃ A-1207 CH₂CF₃ Me F 1 CH₂CH₂CH₂SiMe₃ A-1208 CH₂CF₃ Cl F 1 CH₂CH₂CH₂SiMe₃ A-1209 CH₂CF₃ Me H 1 CH₂CH₂CH₂SiMe₃ A-1210 CH₂CF₃ Me F 0 CH₂CH₂CH₂CH₂SiMe₃ A-1211 CH₂CF₃ Me F 1 CH₂CH₂CH₂CH₂SiMe₃ A-1212 CH₂CF₃ Cl F 0 CH₂CH₂CH₂CH₂SiMe₃ A-1213 CH₂CF₃ Cl F 1 CH₂CH₂CH₂CH₂SiMe₃ A-1214 CH₂CF₃ Cl F 1 SO₂CH₂Ph A-1215 CH₂CF₃ Me F 1 C(═O)Ph A-1216 CH₂CF₃ Me F 0 C(═O)Ph A-1217 CH₂CF₃ Cl F 0 C(═O)Ph A-1218 CH₂CF₃ Cl F 1 C(═O)Ph

TABLE 32 [I]

Compound No. R¹ R² R³ n R⁴ B-0001 CH₂CF₃ Me F 0

B-0002 CH₂CF₃ Me F 1

B-0003 CH₂CF₃ Me F 0

B-0004 CH₂CF₃ Me F 1

B-0005 CH₂CF₃ Me F 0

B-0006 CH₂CF₃ Me F 1

B-0007 CH₂CF₃ Me F 0

B-0008 CH₂CF₃ Me F 1

B-0009 CH₂CF₃ Me F 1

B-0010 CH₂CF₃ Me F 0

TABLE 33 Compound No. R¹ R² R³ n R⁴ B-0011 CH₂CF₃ Me F 1

B-0012 CH₂CF₃ Me F 0

B-0013 CH₂CF₃ Me F 1

B-0014 CH₂CF₃ Cl F 0

B-0015 CH₂CF₃ Cl F 1

B-0016 CH₂CF₃ Cl F 0

B-0017 CH₂CF₃ Me F 0

B-0018 CH₂CF₃ Me F 1

B-0019 CH₂CF₃ Me F 1

B-0020 CH₂CF₃ Me F 0

B-0021 CH₂CF₃ Me F 1

B-0022 CH₂CF₃ Me F 0

TABLE 34 Compound No. R¹ R² R³ n R⁴ B-0023 CH₂CF₃ Me F 1

B-0024 CH₂CF₃ Me F 0

B-0025 CH₂CF₃ Me F 1

B-0026 CH₂CF₃ Me F 1

B-0027 CH₂CF₃ Me F 1

B-0028 CH₂CF₃ Me F 0

B-0029 CH₂CF₃ Me F 0

B-0030 CH₂CF₃ Me F 1

B-0031 CH₂CF₃ Me F 0

B-0032 CH₂CF₃ Me F 1

B-0033 CH₂CF₃ Me F 0

TABLE 35 Compound No. R¹ R² R³ n R⁴ B-0034 CH₂CF₃ Me F 1

B-0035 CH₂CF₃ Me F 0

B-0036 CH₂CF₃ Me H 0

B-0037 CH₂CF₃ Me H 1

B-0038 CH₂CF₃ CHF₂ H 0

B-0039 CH₂CF₃ CHF₂ H 1

B-0040 CH₂CF₃ Me F 2

B-0041 CH₂CF₃ Me F 1

B-0042 CH₂CF₃ Me F 0

B-0043 CH₂CF₃ Cl F 0

B-0044 CH₂CF₃ Cl F 1

B-0045 CH₂CF₃ CN F 0

TABLE 36 Compound No. R¹ R² R³ n R⁴ B-0046 CH₂CF₃ CN F 1

B-0047 CH₂CF₃ Me F 1

B-0048 CH₂CF₃ Me F 0

B-0049 CH₂CF₃ Me F 1

B-0050 CH₂CF₃ Me F 1

B-0051 CH₂CF₃ Me F 0

B-0052 CH₂CF₃ Me F 1

B-0053 CH₂CF₃ Me F 0

B-0054 CH₂CF₃ Me F 1

B-0055 CH₂CF₃ Me F 0

B-0056 CH₂CF₃ Me F 1

B-0057 CH₂CF₃ Me F 0

TABLE 37 Compound No. R¹ R² R³ n R⁴ B-0058 CH₂CF₃ Me F 1

B-0059 CH₂CF₃ Me F 1

B-0060 CH₂CF₃ Me F 0

B-0061 CH₂CF₃ Me F 1

B-0062 CH₂CF₃ Me F 1

B-0063 CH₂CF₃ Me F 0

B-0064 CH₂CF₃ Me F 0

B-0065 CH₂CF₃ Me F 1

B-0066 CH₂CF₃ Me F 0

B-0067 CH₂CF₃ Me F 1

B-0068 CH₂CF₃ Cl F 0

B-0069 CH₂CF₃ Cl F 1

TABLE 38 Compound No. R¹ R² R³ n R⁴ B-0070 CH₂CF₃ Me F 0

B-0071 CH₂CF₃ Me F 1

B-0072 CH₂CF₃ Cl F 0

B-0073 CH₂CF₃ Cl F 1

B-0074 CH₂CF₃ Me F 0

B-0075 CH₂CF₃ Me F 1

B-0076 CH₂CF₃ Me F 0

B-0077 CH₂CF₃ Me F 1

B-0078 CH₂CF₃ Cl F 0

B-0079 CH₂CF₃ Cl F 1

B-0080 CH₂CF₃ Cl F 0

B-0081 CH₂CF₃ Cl F 1

TABLE 39 Compound No. R¹ R² R³ n R⁴ B-0082 CH₂CF₃ Me F 0

B-0083 CH₂CF₃ Me F 1

B-0084 CH₂CF₃ Cl F 0

B-0085 CH₂CF₃ Cl F 1

B-0086 CH₂CF₃ Me F 0

B-0087 CH₂CF₃ Me F 1

B-0088 CH₂CF₃ Me F 0

B-0089 CH₂CF₃ Me F 1

B-0090 CH₂CF₃ Cl F 0

B-0091 CH₂CF₃ Cl F 1

B-0092 CH₂CF₃ Cl F 1

B-0093 CH₂CF₃ Me F 0

TABLE 40 Compound No. R¹ R² R³ n R⁴ B-0094 CH₂CF₃ Cl F 0

B-0095 CH₂CF₃ Cl F 1

B-0096 CH₂CF₃ Me F 0

B-0097 CH₂CF₃ Me F 0

B-0098 CH₂CF₃ Me F 1

B-0099 CH₂CF₃ Me F 0

B-0100 CH₂CF₃ Me F 1

B-0101 CH₂CF₃ Me F 0

B-0102 CH₂CF₃ C F 0

B-0103 CH₂CF₃ Cl F 1

B-0104 CH₂CF₃ Me F 0

B-0105 CH₂CF₃ Me F 1

TABLE 41 Compound No. R¹ R² R³ n R⁴ B-0106 CH₂CF₃ Cl F 0

B-0107 CH₂CF₃ Cl F 1

B-0108 CH₂CF₃ Me F 0

B-0109 CH₂CF₃ Me F 0

B-0110 CH₂CF₃ Me F 1

B-0111 CH₂CF₃ Me F 1

B-0112 CH₂CF₃ Me F 1

B-0113 CH₂CF₃ Me F 0

B-0114 CH₂CF₃ Cl F 0

B-0115 CH₂CF₃ Me F 0

B-0116 CH₂CF₃ Cl F 0

B-0117 CH₂CF₃ Cl F 0

TABLE 42 [I′]

Compound No. R¹ R² R³ n C-0001 CH₂CF₃ Me F 0 C-0002 CH₂CF₃ Me F 1 C-0003 CH₂CF₃ Cl F 0 C-0004 CH₂CF₃ Cl F 1 C-0005 CH₂CF₃ Me H 0 C-0006 CH₂CF₃ Me H 1 C-0007 CH₂CF₃ Me Cl 0 C-0008 CH₂CF₃ Me Cl 1 C-0009 CH₂CF₃ Cl H 0 C-0010 CH₂CF₃ CI H 1 C-0011 CH₂CF₃ CN F 0 C-0012 CH₂CF₃ CN F 1 C-0013 CH₂CF₃ OMe F 0 C-0014 CH₂CF₃ Cl Cl 0 C-0015 CH₂CF₃ Cl Cl 1 C-0016 CH₂CF₃ Cl F 2 C-0017 CH₂CF₃ Me Me 0 C-0018 CH₂CF₃ Me Me 1

The present compound represented by the general formula [I] and general formula [I′] can be produced by the methods shown below, but the production methods of the present compound are not restricted thereto. Incidentally, for example, “the compound represented by the general formula [I-1]”, “the compound represented by formula [I-1]” and “the compound [I-1]”, mentioned below have the same meaning.

<Production Method 1>

Of the present compounds, a compound represented by the general formula [I-1] can be produced, for example, by the following method.

(In the above formula, L¹ is halogen atom, C₁-C₆ alkylsulfonyloxy group, trifluoromethanesulfonyloxy group, nonafluorobutylsulfonyloxy group, phenylsulfonyloxy group, 4-toluenesulfonyloxy group or SO₂M; M is alkali metal or alkaline earth metal, and the alkali metal is preferably sodium or potassium; and R¹, R², R³ and R⁴ each have the same meaning as given above.)

Thus, the compound represented by the general formula [I-1] can be produced by reacting a compound represented by the general formula [II] with a compound represented by the general formula [III] in an appropriate solvent in the presence or absence of an appropriate base in the presence or absence of an appropriate radical initiator.

The amount of the compound [III] used in the present reaction is selected appropriately, and ordinarily in a range of 1.0 to 5.0 mols and is preferably 1.0 to 2.0 mols relative to 1 mol of the compound [II].

As the solvent usable in the present reaction, there can be mentioned, for example, an ether such as diethyl ether, tetrahydrofuran, 1,4-dioxane or the like; an aromatic hydrocarbon such as benzene, toluene, xylene, chlorobenzene or the like; a halogenated hydrocarbon such as dichloromethane, chloroform, 1,2-dichloroethane or the like; an aprotic polar solvent such as N,N-dimethylformamide, N,N-dimethylacetamide, N-methyl-2-pyrrolidone, dimethyl sulfoxide, sulfolane or the like; an alcohol such as methanol, ethanol, 2-propanol or the like; a nitrile such as acetonitrile, propionitrile or the like; an ester such as ethyl acetate, ethyl propionate or the like; an aliphatic hydrocarbon such as pentane, hexane, cyclohexane, heptane or the like; a pyridine such as pyridine, picoline or the like; water; and a mixture thereof. Incidentally, the use amount of the solvent is 0.1 to 100 liters, preferably 0.3 to 5 liters relative to 1 mol of the compound [II].

As the base usable in the present reaction, there can be mentioned, for example, an inorganic base such as alkali metal hydroxide (e.g. sodium hydroxide or potassium hydroxide), alkaline earth metal hydroxide (e.g. calcium hydroxide or magnesium hydroxide), alkali metal carbonate (e.g. sodium carbonate or potassium carbonate), alkali metal bicarbonate (e.g. sodium hydrogencarbonate or potassium hydrogencarbonate) or the like; a metal hydride (e.g. sodium hydride or potassium hydride); a metal alcoholate (e.g. sodium methoxide, sodium ethoxide or potassium tert-butoxide); and an organic base (e.g. triethylamine, N,N-dimethylaniline, pyridine, 4-N,N-dimethylaminopyridine or 1, 8-diazabicyclo[5.4.0]-7-undecene). Incidentally, the use amount of the base is appropriately selected in a range of 0 to 5.0 mols and is preferably 0 to 1.2 mols relative to 1 mol of the compound [II].

As the radical initiator usable in the present reaction, there can be mentioned, for example, sulfurous acid, sodium sulfite, potassium sulfite, sodium hydrogensulfite, potassium hydrogensulfite, and a sulfurous acid adduct such as Rongalit (trade name, sodium formaldehyde sulfoxylate). A base and a radical initiator may be used in combination. The use amount of the radical initiator is appropriately selected in a range of 0 to 5.0 mols and is preferably 0 to 1.2 mols relative to 1 mol of the compound [II].

The temperature of the present reaction is selected freely, and ordinarily in a temperature range from −30° C. to the reflux temperature of the reaction system and is preferably 0° C. to 150° C.

The time of the present reaction differs depending upon the temperature of reaction, the substrate of reaction, the amount of reactant, etc., but is ordinarily 10 minutes to 24 hours.

After the completion of the reaction, the reaction mixture is subjected to operations such as pouring into water, extraction with organic solvent, concentration and the like, whereby a compound [I-1] can be isolated. The isolated compound [I-1] may be as necessary purified by column chromatography, recrystallization, etc.

[Production Method 2>

Of the present compounds, the compound represented by the general formula [I-1] can also be produced, for example, by the following method using a compound represented by the general formula [IV].

(In the above formula, L² is halogen atom or SO₂M; and R¹, R², R³, R⁴ and M each have the same meaning as given above.)

The compound represented by the general formula [I-1] can be produced by reacting a compound [IV] with a compound [V] in an appropriate solvent in the presence of an appropriate radical initiator.

The amount of the compound [V] used in the present reaction is selected appropriately in a range of 1.0 to 5.0 mols and is preferably 2.0 to 3.0 mols relative to 1 mol of the compound [IV].

As the solvent usable in the present reaction, there can be mentioned, for example, an ether such as diethyl ether, tetrahydrofuran, 1,4-dioxane or the like; an aromatic hydrocarbon such as benzene, toluene, xylene, chlorobenzene or the like; an aprotic polar solvent such as N,N-dimethylformamide, N,N-dimethylacetamide, N-methyl-2-pyrrolidone, dimethyl sulfoxide, sulfolane or the like; a nitrite such as acetonitrile, propionitrile or the like; an ester such as ethyl acetate, ethyl propionate or the like; an aliphatic hydrocarbon such as pentane, hexane, cyclohexane, heptane or the like; a pyridine such as pyridine, picoline or the like; water; and a mixture thereof. Incidentally, the use amount of the solvent is 0.1 to 100 liters, preferably 0.3 to 5 liters relative to 1 mol of the compound [IV].

As the radical initiator usable in the present reaction, there can be mentioned, for example, sulfurous acid, sodium sulfite, potassium sulfite, sodium hydrogensulfite, potassium hydrogensulfite, and a sulfurous acid adduct such as Rongalit (trade name, sodium formaldehyde sulfoxylate). The use amount of the radical initiator is appropriately selected in a range of 0.01 to 5.0 mols and is preferably 0.05 to 1.2 mols relative to 1 mol of the compound [IV].

The temperature of the present reaction is selected freely, and ordinarily in a temperature range from −30° C. to the reflux temperature of the reaction system and is preferably 0° C. to 150° C.

The time of the present reaction differs depending upon the temperature of reaction, the substrate of reaction, the amount of reactant, etc., but is ordinarily 10 minutes to 24 hours.

After the completion of the reaction, the reaction mixture is subjected to operations such as pouring into water, extraction with organic solvent, concentration and the like, whereby a compound [I-1] can be isolated. The isolated compound [I-1] may be as necessary purified by column chromatography, recrystallization, etc.

[Production Method 3>

Of the present compounds, the compound represented by the general formula [I-1′] can also be produced, for example, by the following method using a compound represented by the general formula [VI].

(In the above formula, R¹⁰ is electron withdrawing group such as trifluoromethyl group, nitro group, cyano group or the like; R¹, R³ and R⁴ each have the same meaning as given above; L³ is halogen atom, C₁-C₆ alkylsulfonyloxy group, trifluoromethanesulfonyloxy group, nonafluorobutylsulfonyloxy group, phenylsulfonyloxy group, 4-toluenesulfonyloxy group, C₁-C₆ alkylsulfonyl group or phenylsulfonyl group.)

The compound represented by the general formula [I-1′] can be produced by reacting a compound [VI] with a compound [VII] in an appropriate solvent in the presence of any of an appropriate base, copper and copper oxide (I), or in the presence of an appropriate base and copper, or in the presence of an appropriate base and copper oxide (I).

The amount of the compound [VII] used in the present reaction is selected appropriately in a range of 1.0 to 5.0 mols and is preferably 1.0 to 1.2 mols relative to 1 mol of the compound [VI].

As the solvent usable in the present reaction, there can be mentioned, for example, an ether such as diethyl ether, tetrahydrofuran, 1,4-dioxane or the like; an aromatic hydrocarbon such as benzene, toluene, xylene, chlorobenzene or the like; an aprotic polar solvent such as N,N-dimethylformamide, N,N-dimethylacetamide, N-methyl-2-pyrrolidone, dimethyl sulfoxide, sulfolane or the like; an alcohol such as methanol, ethanol, 2-propanol, methyl cellosolve or the like; an aliphatic hydrocarbon such as pentane, hexane, cyclohexane, heptane or the like; a pyridine such as pyridine, picoline or the like; water; and a mixture thereof. Incidentally, the use amount of the solvent is 0.1 to 100 liters, preferably 0.3 to 10 liters relative to 1 mol of the compound [VI].

As the base usable in the present reaction, there can be mentioned, for example, an inorganic base such as alkali metal hydroxide (e.g. sodium hydroxide or potassium hydroxide), alkaline earth metal hydroxide (e.g. calcium hydroxide or magnesium hydroxide), alkali metal carbonate (e.g. sodium carbonate or potassium carbonate), alkali metal bicarbonate (e.g. sodium hydrogencarbonate or potassium hydrogencarbonate) or the like; a metal hydride (e.g. sodium hydride or potassium hydride); a metal alcoholate (e.g. sodium methoxide, sodium ethoxide or potassium tert-butoxide); and an organic base (e.g. triethylamine, N,N-dimethylaniline, pyridine, 4-N,N-dimethylaminopyridine or 1,8-diazabicyclo[5.4.0]-7-undecene).

The amounts of the base, copper and copper oxide (I) used in the present reaction are each selected appropriately in a range of 1.0 to 5.0 mols and are preferably 1.0 to 1.2 mols relative to 1 mol of the compound [VI].

The temperature of the present reaction is selected freely, and ordinarily in a temperature range from −70° C. to the reflux temperature of the reaction system and is preferably 0° C. to 150° C.

The time of the present reaction differs depending upon the temperature of reaction, the substrate of reaction, the amount of reactant, etc., but is ordinarily 10 minutes to 24 hours.

After the completion of the reaction, the reaction mixture is subjected to operations such as pouring into water, extraction with organic solvent, concentration and the like, whereby a compound [I-1] can be isolated. The isolated compound [I-1′] may be as necessary purified by column chromatography, recrystallization, etc.

[Production Method 4]

Of the present compounds, a compound represented by the general formula [I-1] can also be produced, for example, by a method represented by the following reaction formula using a compound represented by the general formula [VIII].

(In the above formula, R¹, R², R³, R⁴ and M each have the same meaning as given above.)

The compound represented by the general formula [I-1] can be produced by converting a compound [VIII] to a diazonium salt in an appropriate solvent based on the method described in Organic Syntheses Coll., Vol. 3, p. 185 (1955) (for example, a method of using a mineral acid (e.g. hydrochloric acid or sulfuric acid) and a nitrous acid salt or an alkyl nitrite) and then reacting the diazonium salt with a mercaptan salt represented by a compound [IX] or a disulfide represented by a compound [X].

The amount of the compound [IX] or the compound [X] used in the present reaction is appropriately selected in a range of 0.3 to 5.0 mols and is preferably 0.5 to 2.0 mols relative to 1 mol of the compound [VIII].

As the solvent usable in the present reaction, there can be mentioned, for example, an ether such as diethyl ether, tetrahydrofuran, 1,4-dioxane or the like; an aromatic hydrocarbon such as benzene, toluene, xylene, chlorobenzene or the like; a halogenated hydrocarbon such as dichloromethane, chloroform, 1,2-dichloroethane or the like; an aprotic polar solvent such as N,N-dimethylformamide, N,N-dimethylacetamide, N-methyl-2-pyrrolidone, dimethyl sulfoxide, sulfolane or the like; an alcohol such as methanol, ethanol, 2-propanol or the like; a nitrile such as acetonitrile, propionitrile or the like; an ester such as ethyl acetate, ethyl propionate or the like; an aliphatic hydrocarbon such as pentane, hexane, cyclohexane, heptane or the like; a pyridine such as pyridine, picoline or the like; water; and a mixture thereof. Incidentally, the use amount of the solvent is 0.1 to 100 liters, preferably 0.3 to 10 liters relative to 1 mol of the compound [VIII].

The temperature of the present reaction is selected freely, and ordinarily in a temperature range from −30° C. to the reflux temperature of the reaction system and is preferably −10° C. to 100° C.

The time of the present reaction differs depending upon the temperature of reaction, the substrate of reaction, the amount of reactant, etc., but is ordinarily 10 minutes to 24 hours.

After the completion of the reaction, the reaction mixture is subjected to operations such as pouring into water, extraction with organic solvent, concentration and the like, whereby a compound [I-1] can be isolated. The isolated compound [I-1] may be as necessary purified by column chromatography, recrystallization, etc.

<Production Method 5>

Of the present compounds, a compound represented by the general formula [I-1] can also be produced, for example, by a method represented by the following reaction formula using a compound represented by the general formula [XI].

(In the above formula, Y¹ is hydrogen atom or a halogen atom; and L³, R¹, R², R³ and R⁴ each have the same meaning as given above.)

The compound represented by the general formula [I-1] can be produced by reacting a compound [XI] with a metal or an organometallic compound in an appropriate solvent and then reacting the reaction product with a compound [XII] or a compound [X].

As the metal usable in the present reaction, there can be mentioned an alkali metal such as lithium, sodium, potassium or the like; an alkaline earth metal such as magnesium or the like; and so forth.

As the organometallic compound usable in the present reaction, there can be mentioned an alkyl lithium such as n-butyl lithium or the like; and so forth.

The amount of the metal or organometallic compound used in the present reaction is appropriately selected in a range of 1.0 to 3.0 mols and is preferably 1.0 to 1.1 mols relative to 1 mol of the compound [XI].

The amount of the compound [XII] or compound [X] used in the present reaction is appropriately selected in a range of 0.3 to 5.0 mols and is preferably 0.5 to 2.0 mols relative to 1 mol of the compound [XI].

As the solvent usable in the present reaction, there can be mentioned, for example, an ether such as diethyl ether, tetrahydrofuran, 1,4-dioxane or the like; an aromatic hydrocarbon such as benzene, toluene, xylene, chlorobenzene or the like; an aliphatic hydrocarbon such as pentane, hexane, cyclohexane, heptane or the like; a pyridine such as pyridine, picoline or the like; and a mixed solvent thereof. Incidentally, the use amount of the solvent is 0.1 to 100 liters, preferably 0.3 to 10 liters relative to 1 mol of the compound [XI].

The temperature of the present reaction is selected freely, and ordinarily in a temperature range from −100° C. to the reflux temperature of the reaction system and is preferably −78° C. to 100° C.

The time of the present reaction differs depending upon the temperature of reaction, the substrate of reaction, the amount of reactant, etc., but is ordinarily 10 minutes to 24 hours.

After the completion of the reaction, the reaction mixture is subjected to operations such as pouring into water or the like, extraction with organic solvent, concentration and the like, whereby a compound [I-1] can be isolated. The isolated compound [I-1] may be as necessary purified by column chromatography, recrystallization, etc.

<Production Method 6>

A present compound represented by the general formula [I] can be produced by a method of the following reaction formula.

(In the above formula, L¹, R¹, R², R³, R⁴ and n each have the same meaning as given above.)

The present compound can be produced by reacting a compound [I′-1] with a compound [XIII] in an appropriate solvent in the presence of an appropriate base.

The amount of the compound [XIII] used in the present reaction is appropriately selected in a range of 1.0 to 5.0 mols and is preferably 1.0 to 2.0 mols relative to 1 mol of the compound [I′-1].

As the solvent usable in the present reaction, there can be mentioned, for example, an ether such as diethyl ether, tetrahydrofuran, 1,4-dioxane or the like; an aromatic hydrocarbon such as benzene, toluene, xylene, chlorobenzene or the like; a halogenated hydrocarbon such as dichloromethane, chloroform, 1,2-dichloroethane or the like; an aprotic polar solvent such as N,N-dimethylformamide, N,N-dimethylacetamide, N-methyl-2-pyrrolidone, dimethyl sulfoxide, sulfolane or the like; an alcohol such as methanol, ethanol, 2-propanol or the like; a nitrile such as acetonitrile, propionitrile or the like; an ester such as ethyl acetate, ethyl propionate or the like; an aliphatic hydrocarbon such as pentane, hexane, cyclohexane, heptane or the like; a pyridine such as pyridine, picoline or the like; water; and a mixture thereof. Incidentally, the use amount of the solvent is 0.1 to 100 liters, preferably 0.1 to 15 liters relative to 1 mol of the compound [I′-1].

As the base usable in the present reaction, there can be mentioned, for example, an inorganic base such as alkali metal hydroxide (e.g. sodium hydroxide or potassium hydroxide), alkaline earth metal hydroxide (e.g. calcium hydroxide or magnesium hydroxide), alkali metal carbonate (e.g. sodium carbonate or potassium carbonate), alkali metal bicarbonate (e.g. sodium hydrogencarbonate or potassium hydrogencarbonate) or the like; a metal hydride (e.g. sodium hydride or potassium hydride); a metal alcoholate (e.g. sodium methoxide, sodium ethoxide or potassium tert-butoxide); and an organic base (e.g. triethylamine, N,N-dimethylaniline, pyridine, 4-N,N-dimethylaminopyridine or 1,8-diazabicyclo[5.4.0]-7-undecene). Incidentally, the use amount of the base is appropriately selected in a range of 1.0 to 5.0 mols and is preferably 1.0 to 1.5 mols relative to 1 mol of the compound [I′-1].

The temperature of the present reaction is selected freely, and ordinarily in a temperature range from −30° C. to the reflux temperature of the reaction system and is preferably 0° C. to 150° C.

The time of the present reaction differs depending upon the temperature of reaction, the substrate of reaction, the amount of reactant, etc., but is ordinarily 10 minutes to 24 hours.

After the completion of the reaction, the reaction mixture is subjected to operations such as pouring into water or the like, extraction with organic solvent, concentration and the like, whereby a compound [I] can be isolated. The isolated compound [I] may be as necessary purified by column chromatography, recrystallization, etc.

<Production Method 7>

A present compound represented by the general formula [I] can also be produced by a method of the following reaction formula.

(In the above formula, R¹, R², R³, R⁴ and n each have the same meaning as given above.)

The present compound can be produced by reacting a compound [I′-1] with a compound [XIV] in an appropriate solvent in the presence of a tri-substituted phosphine and an azodicarboxylic acid derivative or in the presence of phosphorane.

The amount of the compound [XIV] used in the present reaction is appropriately selected in a range of 1.0 to 5.0 mols and is preferably 1.0 to 2.0 mols relative to 1 mol of the compound [I′-1].

As the solvent usable in the present reaction, there can be mentioned, for example, an ether such as diethyl ether, tetrahydrofuran, 1,4-dioxane or the like; an aromatic hydrocarbon such as benzene, toluene, xylene, chlorobenzene or the like; an aprotic polar solvent such as N,N-dimethylformamide, N,N-dimethylacetamide, N-methyl-2-pyrrolidone, dimethyl sulfoxide, sulfolane or the like; an alcohol such as methanol, ethanol, 2-propanol or the like; a halogenated hydrocarbon such as dichloromethane, chloroform, 1,2-dichloroethane or the like; an aliphatic hydrocarbon such as pentane, hexane, cyclohexane, heptane or the like; a ketone such as acetone, methyl ethyl ketone, cyclohexanone or the like; acetic acid; water; and a mixed solvent thereof. Incidentally, the use amount of the solvent is 0.1 to 100 liters, preferably 0.3 to 30 liters relative to 1 mol of the compound [I′-1].

As the tri-substituted phosphine usable in the present reaction, there can be mentioned, for example, triphenylphosphine, tributylphosphine, and trimethylphosphine. Incidentally, the use amount of the tri-substituted phosphine is appropriately selected in a range of 1.0 to 5.0 mols and is preferably 1.0 to 3.0 mols relative to 1 mol of the compound [I′-1].

As the azodicarboxylic acid derivative usable in the present reaction, there can be mentioned, for example, diethyl azodicarboxylate, diisopropyl azodicarboxylate, dimethoxyethyl azodicarboxylate, and N,N,N′,N′-tetramethylazodicarboxylic acid amide. Incidentally, the use amount of the azodicarboxylic acid derivative is appropriately selected in a range of 1.0 to 5.0 mols and is preferably 1.0 to 2.0 mols relative to 1 mol of the compound [I′-1].

As the phosphorane usable in the present reaction, there can be mentioned, for example, cyanomethylenetrimethylphosphorane and cyanomethylenetributylphosphorane. Incidentally, the use amount of the phosphorane is appropriately selected in a range of 1.0 to 5.0 mols and is preferably 1.0 to 2.0 mols relative to 1 mol of the compound [I′-1].

The temperature of the present reaction is selected freely, and ordinarily in a temperature range from −30° C. to the reflux temperature of the reaction system and is preferably 0° C. to 150° C.

The time of the present reaction differs depending upon the temperature of reaction, the substrate of reaction, the amount of reactant, etc., but is ordinarily 10 minutes to 24 hours.

After the completion of the reaction, the reaction mixture is subjected to operations such as pouring into water or the like, extraction with organic solvent, concentration and the like, whereby a compound [I] can be isolated. The isolated compound [I] may be as necessary purified by column chromatography, recrystallization, etc.

<Production Method 8>

Of the present compounds represented by the general formula [I], a compound represented by the general formula [I-2] can be produced, for example, by a method represented by the following reaction formula using a compound represented by the general formula [I-1].

(In the above formula, R¹, R², R³ and R⁴ each have the same meaning as given above; and m is an integer of 1 or 2.)

The compound represented by the general formula [I-2] can be produced by reacting a compound [I-1] with an oxidizing agent in an appropriate solvent in the presence or absence of an appropriate catalyst.

As the oxidizing agent usable in the present reaction, there can be mentioned, for example, hydrogen peroxide, m-chloroperbenzoic acid, sodium periodate, OXONE (trade name of E.I. DuPont, a substance containing potassium hydrogenperoxosulfate), N-chlorosuccinimide, N-bromosuccinimide, tert-butyl hypochlorite, and sodium hypochlorite. Incidentally, the use amount of the oxidizing agent depends upon the oxidation number m of the sulfur atom of the compound represented by the general formula [I-2], but is appropriately selected in a range of 1.0 to 5.0 mols and is preferably 0.5 to 2.5 mols relative to 1 mol of the compound [I-1].

As the catalyst usable in the present reaction, there can be mentioned, for example, sodium tungstate. Incidentally, the use amount of the catalyst is appropriately selected in a range of 0 to 1.0 mol and is preferably 0 to 0.1 mol relative to 1 mol of the compound [I-1].

As the solvent usable in the present reaction, there can be mentioned, for example, an ether such as diethyl ether, tetrahydrofuran, 1,4-dioxane or the like; an aromatic hydrocarbon such as benzene, toluene, xylene, chlorobenzene or the like; an aprotic polar solvent such as N,N-dimethylformamide, N,N-dimethylacetamide, N-methyl-2-pyrrolidone, dimethyl sulfoxide, sulfolane or the like; an alcohol such as methanol, ethanol, 2-propanol or the like; a halogenated hydrocarbon such as dichloromethane, chloroform, 1,2-dichloroethane or the like; an aliphatic hydrocarbon such as pentane, hexane, cyclohexane, heptane or the like; a ketone such as acetone, methyl ethyl ketone, cyclohexanone or the like; acetic acid; water; and a mixed solvent thereof. Incidentally, the use amount of the solvent is 0.1 to 100 liters, preferably 0.3 to 45 liters relative to 1 mol of the compound [I-1].

The temperature of the present reaction is selected freely, and ordinarily in a temperature range from −30° C. to the reflux temperature of the reaction system and is preferably −10° C. to 100° C.

The time of the present reaction differs depending upon the temperature of reaction, the substrate of reaction, the amount of reactant, etc., but is ordinarily 10 minutes to 24 hours.

After the completion of the reaction, the reaction mixture is subjected to operations such as pouring into water or the like, extraction with organic solvent, concentration and the like, whereby a compound [I-2] can be isolated. The isolated compound [I-2] may be as necessary purified by column chromatography, recrystallization, etc.

<Production Method 9>

A present compound represented by the general formula [I′] can be produced, for example, by the method shown by the following reaction formula using a compound represented by the general formula [XV-2].

(In the above formula, R^(1′), R^(2′), R^(3′) and n each have the same meaning as give above.)

The compound represented by the general formula [I′] can be produced by reacting the compound [XV-2] with an acid and a nitrous acid derivative in a solvent and then, as necessary, reacting the reaction product with a metal salt.

As the acid usable in the present reaction, there can be mentioned a mineral acid such as sulfuric acid, nitric acid or the like, or an organic acid such as trifluoroacetic acid, trifluoromethanesulfonic acid or the like. Incidentally, the use amount of the acid is appropriately selected in a range of 1 to 20 mols and is preferably 1.0 to 5.0 mols relative to 1 mol of the compound [XV-2].

As the nitrous acid derivative usable in the present reaction, there can be mentioned a nitrous acid salt such as sodium nitrite, potassium nitrite or the like, or an alkyl nitrite such as n-butyl nitrite, isopentyl nitrite, tert-butyl nitrite or the like. Incidentally, the use amount of the nitrous acid derivative is appropriately selected in a range of 1.0 to 3.0 mols and is preferably 1.0 to 1.5 mols relative to 1 mol of the compound [XV-2].

As the metal salt as necessary usable in the present reaction, there can be mentioned copper sulfate, copper nitrate, copper oxide, etc. Incidentally, the use amount of the metal salt is appropriately selected in a range of 0 to 2.0 mols and is preferably 0 to 1.1 mols relative to 1 mol of the compound [XV-2].

As the solvent usable in the present reaction, there can be mentioned, for example, an ether such as diethyl ether, tetrahydrofuran, 1,4-dioxane or the like; an aromatic hydrocarbon such as benzene, toluene, xylene, chlorobenzene or the like; a halogenated hydrocarbon such as dichloromethane, chloroform, dichloroethane or the like; an aprotic polar solvent such as N,N-dimethylformamide, N,N-dimethylacetamide, N-methyl-2-pyrrolidone, dimethyl sulfoxide, sulfolane or the like; an alcohol such as methanol, ethanol, 2-propanol or the like; a nitrile such as acetonitrile, propionitrile or the like; an ester such as ethyl acetate, ethyl propionate or the like; an aliphatic hydrocarbon such as pentane, hexane, cyclohexane, heptane or the like; a pyridine such as pyridine, picoline or the like; water; and a mixed solvent thereof. Incidentally, the use amount of the solvent is 0.1 to 100 liters, preferably 0.3 to 10 liters relative to 1 mol of the compound [XV-2].

The temperature of the present reaction is selected freely in a temperature range from −30° C. to the reflux temperature of the reaction system and is preferably 0° C. to 150° C.

The time of the present reaction differs depending upon the temperature of reaction, the substrate of reaction, the amount of reactant, etc., but is ordinarily 10 minutes to 24 hours.

After the completion of the reaction, the reaction mixture is subjected to operations such as pouring into water or the like, extraction with organic solvent, concentration and the like, whereby a compound [I′] can be isolated. The isolated compound [I′] may be as necessary purified by column chromatography, recrystallization, etc.

<Production Method 10>

The present compound represented by the general formula [I′] can also be produced by the method shown by the following reaction formula.

(In the above formula, R¹¹ is boronic acid (—B(OH)₂ group) or pinacolateboran-2-yl group; R^(1′), R^(2′), R^(3′) and n each have the same meaning as given above.)

The compound represented by the general formula [I′] can be produced by reacting a compound [XVI-1] with an oxidizing agent in a solvent.

As the oxidizing agent usable in the present reaction, there can be mentioned, for example, hydrogen peroxide and 4-methylmorpholine-N-oxide. Incidentally, the use amount of the oxidizing agent is appropriately selected in a range of 1.0 to 6.0 mols and is preferably 1.0 to 1.4 mols relative to 1 mol of the compound [XVI-1].

As the solvent usable in the present reaction, there can be mentioned, for example, an ether such as diethyl ether, tetrahydrofuran, 1,4-dioxane or the like; an aromatic hydrocarbon such as benzene, toluene, xylene, chlorobenzene or the like; an aprotic polar solvent such as N,N-dimethylformamide, N,N-dimethylacetamide, N-methyl-2-pyrrolidone, dimethyl sulfoxide, sulfolane or the like; an alcohol such as methanol, ethanol, 2-propanol or the like; a halogenated hydrocarbon such as dichloromethane, chloroform, 1,2-dichloroethane or the like; an aliphatic hydrocarbon such as pentane, hexane, cyclohexane, heptane or the like; a ketone such as acetone, methyl ethyl ketone, cyclohexanone or the like; acetic acid; water; and a mixed solvent thereof. Incidentally, the use amount of the solvent is 0.1 to 100 liters, preferably 0.3 to 15 liters relative to 1 mol of the compound [XVI-1].

The temperature of the present reaction is selected freely in a temperature range from −30° C. to the reflux temperature of the reaction system and is preferably −10° C. to 150° C.

The time of the present reaction differs depending upon the temperature of reaction, the substrate of reaction, the amount of reactant, etc., but is ordinarily 10 minutes to 24 hours.

After the completion of the reaction, the reaction mixture is subjected to operations such as pouring into water or the like, extraction with organic solvent, concentration and the like, whereby a compound [I′] can be isolated. The isolated compound [I′] may be as necessary purified by column chromatography, recrystallization, etc.

<Production Method 11>

Of the present compounds represented by the general formula [I], the compound represented by the general formula [I-4] can be produced, for example, by the method shown by the following reaction formula, using a compound represented by the general formula [I-3].

(In the above formula, L⁴ is a halogen atom, methanesulfonyloxy group, trifluoromethanesulfonyloxy group, 1,1,2,2,3,3,4,4,4-nonafluorobutylsulfonyloxy group, 4-toluenesulfonyloxy group or benzenesulfonyloxy group; R¹² is hydrogen atom, cyano group, C₁-C₆ alkyl group, C₁-C₆ haloalkyl group, C₃-C₈ cycloalkyl C₁-C₆ alkyl group, C₃-C₈ halocycloalkyl C₁-C₆ alkyl group, C₃-C₈ cycloalkyl group or C₃-C₈ halocycloalkyl group; p is an integer of 1-12; R¹, R², R³ and n each have the same meaning as given above.)

The compound represented by the general formula [I-4] can be produced by reacting a compound [I-3] and sulfide in an appropriate solvent in the presence or absence of base.

As the sulfide usable in the present reaction, there can be mentioned, for example, hydrosulfide of alkali metal such as sodium hydrosulfide or potassium hydrosulfide; thiocyanate of alkali metal such as sodium thiocyanate or potassium thiocyanate; alkylmercaptane such as methyl mercaptane, ethyl mercaptane or tert-butyl mercaptane; haloalkylmercaptane such as 2,2,2-trifluoroethyl mercaptane; and cycloalkylalkylmercaptane such as cyclopropylmethyl mercaptane. Incidentally, the use amount of the sulfide is appropriately selected in a range of 1.0 to 20 mols and is preferably 1.0 to 10 mols relative to 1 mol of the compound [I-3].

As the base usable in the present reaction, there can be mentioned, for example, an inorganic base such as alkali metal hydroxide (e.g. sodium hydroxide or potassium hydroxide), alkaline earth metal hydroxide (e.g. calcium hydroxide or magnesium hydroxide), alkali metal carbonate (e.g. sodium carbonate or potassium carbonate), alkali metal bicarbonate (e.g. sodium hydrogencarbonate or potassium hydrogencarbonate) or the like; a metal hydride (e.g. sodium hydride or potassium hydride); a metal alcoholate (e.g. sodium methoxide, sodium ethoxide or potassium tert-butoxide); and an organic base (e.g. triethylamine, N,N-dimethylaniline, pyridine, 4-N,N-dimethylaminopyridine or 1,8-diazabicyclo[5.4.0]-7-undecene). Incidentally, the use amount of the base is appropriately selected in a range of 1.0 to 5.0 mols and is preferably 1.0 to 2.0 mols relative to 1 mol of the compound [I-3].

As the solvent usable in the present reaction, there can be mentioned, for example, an ether such as diethyl ether, tetrahydrofuran, 1,4-dioxane or the like; an aromatic hydrocarbon such as benzene, toluene, xylene, chlorobenzene or the like; an aprotic polar solvent such as N,N-dimethylformamide, N,N-dimethylacetamide, N-methyl-2-pyrrolidone, dimethyl sulfoxide, sulfolane or the like; an alcohol such as methanol, ethanol, 2-propanol or the like; a nitrile such as acetonitrile, propionitrile or the like; an aliphatic hydrocarbon such as pentane, hexane, cyclohexane, heptane or the like; a pyridine such as pyridine, picoline or the like; and a mixture thereof. Incidentally, the use amount of the solvent is 0.1 to 100 liters, preferably 0.3 to 10 liters relative to 1 mol of the compound [I-3].

The temperature of the present reaction is selected freely in a temperature range from 0° C. to the reflux temperature of the reaction system and is preferably room temperature to 150° C.

The time of the present reaction differs depending upon the temperature of reaction, the substrate of reaction, the amount of reactant, etc., but is ordinarily 10 minutes to 24 hours.

In conducting the present reaction, potassium iodide may be added, and the use amount of potassium iodide is 0 to 5.0 mol, preferably 0 to 1.0 mol relative to 1 mol of the compound [I-3].

After the completion of the reaction, the reaction mixture is subjected to operations such as pouring into water or the like, extraction with organic solvent, concentration and the like, whereby a compound [I-4] can be isolated. The isolated compound [I-4] may be as necessary purified by column chromatography, recrystallization, etc.

<Production Method 12>

Of the present compounds represented by the general formula [I], the compound represented by the general formula [I-6] can be produced by, for example, the method shown by the following reaction formula, using a compound represented by the general formula [I-5].

(In the above formula, R¹, R², R³, n and p each have the same meaning as given above.)

The compound represented by the general formula [I-6] can be produced by reacting a compound [I-5] and trifluoromethylating agent in an appropriate solvent in the presence of an appropriate catalyst.

As the trifluoromethylating agent usable in the present reaction, there can be mentioned, for example, trifluoromethyltrimethylsilane or triethyltrifluoromethylsilane. Incidentally, the use amount of the trifluoromethylating agent is appropriately selected in a range of 1.0 to 5.0 mols and is preferably 1.0 to 3.0 mols relative to 1 mol of the compound [I-5].

As the catalyst usable in the present reaction, there can be mentioned, for example, tetra-n-butylammoniumfluoride, cesium fluoride or potassium fluoride. Incidentally, the use amount of the catalyst is appropriately selected in a range of 0.01 to 10 mols and is preferably 0.1 to 6.0 mols relative to 1 mol of the compound [I-5].

As the solvent usable in the present reaction, there can be mentioned, for example, an ether such as diethyl ether, tetrahydrofuran, 1,4-dioxane or the like; an aromatic hydrocarbon such as benzene, toluene, xylene, chlorobenzene or the like; an aprotic polar solvent such as N,N-dimethylformamide, N,N-dimethylacetamide, N-methyl-2-pyrrolidone, dimethyl sulfoxide, sulfolane or the like; a halogenated hydrocarbon such as dichloromethane, chloroform, 1,2-dichloroethane or the like; a nitrile such as acetonitrile, propionitrile or the like; an aliphatic hydrocarbon such as pentane, hexane, cyclohexane, heptane or the like; and a mixture thereof. Incidentally, the use amount of the solvent is 0.1 to 100 liters, preferably 0.3 to 15 liters relative to 1 mol of the compound [I-5].

The temperature of the present reaction is selected freely in a temperature range from −30° C. to the reflux temperature of the reaction system and is preferably 0° C. to room temperature.

The time of the present reaction differs depending upon the temperature of reaction, the substrate of reaction, the amount of reactant, etc., but is ordinarily 10 minutes to 24 hours.

After the completion of the reaction, the reaction mixture is subjected to operations such as pouring into water or the like, extraction with organic solvent, concentration and the like, whereby a compound [I-6] can be isolated. The isolated compound [I-6] may be as necessary purified by column chromatography, recrystallization, etc.

<Production Method 13>

From the compound represented by the general formula [I-7], having asymmetrical sulfur atom, of the present compounds represented by the general formula [I], respective optical isomer (enantiomer) can be separated by optical resolution.

(In the above formula, R¹, R², R³ and R⁴ each have the same meaning as given above.)

From the recemic mixture of compound represented by the general formula [I-7], respective (+)-enantiomer and (−)-enantiomer can be obtained by using a column for high performance liquid chromatography for optical isomer separation.

As the column for high performance liquid chromatography for optical isomer separation usable, there can be mentioned the column already marketed, for example, CHIRAL PAK AD (trade name) manufactured and sold by Daicel Corporation.

As the solvent usable in the optical resolution, there can be mentioned, for example, an aliphatic hydrocarbon such as hexane, heptane or the like; an alcohol such as methanol, ethanol, propanol, 2-propanol, butanol or the like; a halogenated hydrocarbon such as dichloromethane, chloroform, or the like; an ether such as diethyl ether, 1,2-dimethoxyethane, diisopropyl ether, tetrahydrofuran, 1,4-dioxane or the like; an ester such as ethyl acetate or the like; a nitrile such as acetonitrile or the like; an organic acid such as acetic acid, formic acid and the like; water; and a mixture thereof.

The temperature and time of the optical resolution may be changed freely in a wide range. Ordinally temperature is from −20° C. to 60° C., preferably 5° C. to 50° C., and time is 0.01 hour to 50 hours, preferably 0.1 hour to 2 hours.

<Production Method 1 of Intermediate>

A compound represented by the general formula [II] can be produced by each of the reaction formulas shown by the following step 1 to step 4. A compound represented by the general formula [IV] can be produced by the reaction formula shown by the following step 5. Incidentally, the compound [II] and the compound [IV] are interchangeable to each other by an oxidation reaction or a reduction reaction. Further, the compound [II] is also oxidized easily by the oxygen in the air, generating the compound [IV].

(In the above reaction formulas, Z¹ is a methyl group or a trifluoromethyl group; and R², R³, R⁴ and Y¹ each have the same meaning as given above.)

[Step 1]

A compound represented by the general formula [II] can be produced by oxidizing a compound [XVII] with an appropriate oxidizing agent to convert to a corresponding sulfoxide form, then reacting the sulfoxide form with acetic anhydride or trifluoroacetic anhydride to produce a compound [XVIII], thereafter hydrolyzing the compound [XVIII] based on the method described in Chem. Ber., Vol. 43, p. 1407 (1910). The compound [XVIII] may be used in the next reaction without being isolated and purified.

As the oxidizing agent usable in the present step, there can be mentioned, for example, hydrogen peroxide, m-chloroperbenzoic acid, sodium periodate, OXONE (trade name of E.I. DuPont, a substance containing potassium hydrogenperoxosulfate), N-chlorosuccinimide, N-bromosuccinimide, tert-butyl hypochlorite, and sodium hypochlorite. Incidentally, the use amount of the oxidizing agent is appropriately selected in a range of 1.0 to 3.0 mols and is preferably 1.0 to 1.2 mols relative to 1 mol of the compound [XVII].

The amount of the acetic anhydride or trifluoroacetic anhydride used in the present step is selected in a range from 1 mol to an amount sufficient to act as a solvent and is preferably 1.0 to 3.0 mols relative to 1 mol of the compound [XVII]

The reaction temperature of the present step is freely selected, in any reaction, in a range from −10° C. to the reflux temperature of the reaction system and is preferably 0° C. to 50° C.

The reaction time of the present step differs depending upon the temperature of reaction, the substrate of reaction, the amount of reactant, etc., in any reaction, but is ordinarily 5 minutes to 12 hours.

After the completion of the reaction, the reaction mixture is subjected to operations such as pouring into water or the like, extraction with organic solvent, concentration and the like, whereby a compound [II] can be isolated. The isolated compound [II] may be as necessary purified by column chromatography, recrystallization, etc.

[Step 2]

The compound represented by the general formula [II] can also be produced by reacting a compound [XI] with a metal or an organometallic compound in a solvent and then reacting the reaction product with sulfur.

As the solvent usable in the present step, there can be mentioned, for example, an ether such as diethyl ether, tetrahydrofuran, 1,4-dioxane or the like; an aromatic hydrocarbon such as benzene, toluene, xylene, chlorobenzene or the like; an aliphatic hydrocarbon such as pentane, hexane, cyclohexane, heptane or the like; a pyridine such as pyridine, picoline or the like; and a mixture thereof. Incidentally, the use amount of the solvent is 0.1 to 100 liters, preferably 0.1 to 10 liters relative to 1 mol of the compound [XI].

As the metal usable in the present step, there can be mentioned lithium, magnesium, etc. Incidentally, the use amount of the metal is appropriately selected in a range of 1.0 to 3.0 mols and is preferably 1.0 to 1.2 mols relative to 1 mol of the compound [XI].

As the organometallic compound usable in the present step, there can be mentioned an alkyllithium such as n-butyllithium or the like. Incidentally, the use amount of the organometallic compound is appropriately selected in a range of 1.0 to 3.0 mols and is preferably 1.0 to 1.2 mols relative to 1 mol of the compound [XI].

The amount of the sulfur used in the present step is appropriately selected in a range of 1.0 to 5.0 mols and is preferably 1.0 to 2.0 mols relative to 1 mol of the compound [XI].

The reaction temperature of the present step is freely selected in a range from −60° C. to the reflux temperature of the reaction system and is preferably −60° C. to room temperature.

The reaction time of the present step differs depending upon the temperature of reaction, the substrate of reaction, the amount of reactant, etc., but is ordinarily 30 minutes to 12 hours.

After the completion of the reaction, the reaction mixture is subjected to operations such as pouring into water or the like, extraction with organic solvent, concentration and the like, whereby a compound [II] can be isolated. The isolated compound [II] may be as necessary purified by column chromatography, recrystallization, etc.

[Step 3]

The compound represented by the general formula [II] can also be produced by converting a compound [VIII] to a diazonium salt in the same manner as in the above-mentioned Production method 4, then reacting the diazonium salt with a xanthogenic acid salt or a thiocyanic acid salt, thereafter hydrolyzing the reaction product.

As the xanthogenic acid salt usable in the present step, there can be mentioned, for example, sodium ethylxanthogenate, potassium ethylxanthogenate, potassium isopropylxanthogenate, and potassium butylxanthogenate. As the thiocyanic acid salt, there can be mentioned, for example, sodium thiocyanate, potassium thiocyanate, and ammonium thiocyanate. Incidentally, the use amount of the xanthogenic acid salt or thiocyanic acid salt is appropriately selected in a range of 1.0 to 3.0 mols and is preferably 1.0 to 1.5 mols relative to 1 mol of the compound [VIII].

As the solvent usable in the present step, there can be mentioned, for example, an ether such as diethyl ether, tetrahydrofuran, 1,4-dioxane or the like; an aromatic hydrocarbon such as benzene, toluene, xylene, chlorobenzene or the like; a halogenated hydrocarbon such as dichloromethane, chloroform, 1,2-dichloroethane or the like; an aprotic polar solvent such as N,N-dimethylformamide, N,N-dimethylacetamide, N-methyl-2-pyrrolidone, dimethyl sulfoxide, sulfolane or the like; an alcohol such as methanol, ethanol, 2-propanol or the like; a nitrile such as acetonitrile, propionitrile or the like; an ester such as ethyl acetate, ethyl propionate or the like; an aliphatic hydrocarbon such as pentane, hexane, cyclohexane, heptane or the like; a pyridine such as pyridine, picoline or the like; water; and a mixed solvent thereof. Incidentally, the use amount of the solvent is 0.1 to 100 liters, preferably 0.3 to 10 liters relative to 1 mol of the compound [VIII].

The reaction temperature of the present step is freely selected in a range from −70° C. to the reflux temperature of the reaction system and is preferably −20° C. to 100° C.

The reaction time of the present step differs depending upon the temperature of reaction, the substrate of reaction, the amount of reactant, etc., but is ordinarily 10 minutes to 24 hours.

After the completion of the reaction, the reaction mixture is subjected to operations such as pouring into water or the like, extraction with organic solvent, concentration and the like, whereby a compound [II] can be isolated.

The isolated compound [II] may be as necessary purified by column chromatography, recrystallization, etc.

[Step 4]

The compound represented by the general formula

[II] can also be produced by reacting a compound [XIX] with chlorosulfonic acid to obtain a compound [XX] and then reacting the compound [XX] with a reducing agent.

The amount of the chlorosulfonic acid used in the present step is appropriately selected in a range of 2.0 to 10 mols and is preferably 2.2 to 3.5 mols relative to 1 mol of the compound [XIX].

As the reducing agent usable in the present step, there can be mentioned lithium aluminum hydride, a combination of zinc and an acid, a combination of tin and an acid, and a combination of red phosphorus and iodine. Incidentally, the use amount of the reducing agent is appropriately selected in a range of 1.0 to 5.0 mols and is preferably 1.5 to 2.0 mols relative to 1 mol of the compound [XIX].

As the acid usable as a component of the reducing agent in the present step, there can be mentioned a mineral acid such as hydrochloric acid, sulfuric acid or the like.

The reaction temperature of the present step is freely selected, in any reaction, in a range from 0° C. to the reflux temperature of the reaction system and is preferably 0° C. to 100° C.

The reaction time of the present step differs depending upon the temperature of reaction, the substrate of reaction, the amount of reactant, etc., in any reaction, but is ordinarily 10 minutes to 24 hours.

After the completion of the reaction, the reaction mixture is subjected to operations such as pouring into water or the like, extraction with organic solvent, concentration and the like, whereby a compound [II] can be isolated. The isolated compound [II] may be as necessary purified by column chromatography, recrystallization, etc.

[Step 5]

The compound represented by the general formula

[IV] can be produced by reacting a compound [XIX] with disulfur dichloride in a solvent in the presence or absence of a catalyst.

The amount of the disulfur dichloride used in the present step is appropriately selected in a range of 1.0 to 5.0 mols and is preferably 1.0 to 1.5 mols relative to 1 mol of the compound [XIX].

As the catalyst usable in the present step, there can be mentioned, for example, a metal halide such as aluminum chloride, tin (II) chloride, tin (IV) chloride or the like. Incidentally, the use amount of the catalyst is appropriately selected in a range of 0 to 5.0 mols and is preferably 1.0 to 2.0 mols relative to 1 mol of the compound [XIX].

As the solvent usable in the present step, there can be mentioned, for example, a halogenated hydrocarbon such as dichloromethane, chloroform, 1,2-dichloroethane or the like; and an aromatic hydrocarbon such as chlorobenzene, dichlorobenzene or the like. Incidentally, the use amount of the solvent is 0.1 to 100 liters, preferably 0.3 to 10 liters relative to 1 mol of the compound [XIX].

The reaction temperature of the present step is freely selected in a range from −30° C. to the reflux temperature of the reaction system and is preferably −10° C. to 100° C.

The reaction time of the present step differs depending upon the temperature of reaction, the substrate of reaction, the amount of reactant, etc., but is ordinarily 1 to 24 hours.

Further, the compound [II] can be produced by reducing the compound [IV] based on the methods described in Organic Syntheses, Coll. Vol. 2, p. 580 (1943), J. Am. Chem. Soc., 60, 428 (1928), J. Am. Chem. Soc., 79, 2553 (1957), J. Org. Chem., 26, 3436 (1961), and J. Am. Chem. Soc., 96, 6081 (1974).

<Production Method 2 of Intermediate>

Of the compounds represented by the general formula [II], a compound represented by the general formula [II-1] can be produced by the method shown by the following reaction formula.

(In the above reaction formula, R³, R⁴, R¹⁰ and L³ each have the same meaning as given above.)

The compound represented by the general formula [II-1] can be produced by reacting a compound [VI] with sodium sulfide in a solvent in the presence of a base and then neutralizing the reaction product with a mineral acid or the like.

The amount of the sodium sulfide used in the present reaction is appropriately selected in a range of 1.0 to 3.0 mols and is preferably 1.0 to 1.5 mols relative to 1 mol of the compound [VI].

As the solvent usable in the present reaction, there can be mentioned, for example, an ether such as diethyl ether, tetrahydrofuran, 1,4-dioxane or the like; an aromatic hydrocarbon such as benzene, toluene, xylene, chlorobenzene or the like; an aprotic polar solvent such as N,N-dimethylformamide, N,N-dimethylacetamide, N-methyl-2-pyrrolidone, dimethyl sulfoxide, sulfolane or the like; an alcohol such as methanol, ethanol, 2-propanol or the like; a halogenated hydrocarbon such as dichloromethane, chloroform, 1,2-dichloroethane or the like; an aliphatic hydrocarbon such as pentane, hexane, cyclohexane, heptane or the like; a ketone such as acetone, methyl ethyl ketone, cyclohexanone or the like; water; and a mixed solvent thereof. Incidentally, the use amount of the solvent is 0.1 to 100 liters, preferably 0.3 to 10 liters relative to 1 mol of the compound [VI].

As the base usable in the present reaction, there can be mentioned, for example, an inorganic base such as alkali metal hydroxide (e.g. sodium hydroxide or potassium hydroxide), alkaline earth metal hydroxide (e.g. calcium hydroxide or magnesium hydroxide), alkali metal carbonate (e.g. sodium carbonate or potassium carbonate), alkali metal bicarbonate (e.g. sodium hydrogencarbonate or potassium hydrogencarbonate) or the like; a metal hydride (e.g. sodium hydride or potassium hydride); a metal alcoholate (e.g. sodium methoxide, sodium ethoxide or potassium tert-butoxide); and an organic base (e.g. triethylamine, N,N-dimethylaniline, pyridine, 4-N,N-dimethylaminopyridine or 1,8-diazabicyclo[5.4.0]-7-undecene). Incidentally, the use amount of the base is appropriately selected in a range of 1.0 to 5.0 mols and is preferably 1.0 to 1.2 mols relative to 1 mol of the compound [VI].

As the mineral acid usable in the present reaction, there can be mentioned hydrochloric acid, sulfuric acid, etc. The use amount of the mineral acid is appropriately selected in a range of 1.0 to 5.0 mols and is preferably 1.0 to 2.0 mols relative to 1 mol of the compound [VI].

The temperature of the present reaction is selected freely in a temperature range from −30° C. to the reflux temperature of the reaction system, and is preferably −20° C. to 100° C.

The time of the present reaction differs depending upon the temperature of reaction, the substrate of reaction, the amount of reactant, etc., but is ordinarily 10 minutes to 24 hours.

After the completion of the reaction, the reaction mixture is subjected to operations such as pouring into water or the like, extraction with organic solvent, concentration and the like, whereby a compound [II-1] can be isolated. The isolated compound [II-1] may be as necessary purified by column chromatography, recrystallization, etc.

<Production Method 3 of Intermediate>

A compound represented by the general formula [XV] can be produced by the method of the reaction formulas shown by the following [step 6] and [step 7].

(In the above reaction formulas, R¹, R², R³ and n each have the same meaning as given above.)

[Step 6]

A compound represented by the general formula [XXII] can be produced by reacting a compound [XXI] with nitric acid in a solvent in the presence or absence of sulfuric acid.

As the solvent usable in the present step, there can be mentioned, for example, an ether such as diethyl ether, tetrahydrofuran, 1,4-dioxane or the like; an aromatic hydrocarbon such as benzene, toluene, xylene, chlorobenzene or the like; an aprotic polar solvent such as N,N-dimethylformamide, N,N-dimethylacetamide, N-methyl-2-pyrrolidone, dimethyl sulfoxide, sulfolane or the like; an alcohol such as methanol, ethanol, 2-propanol or the like; a halogenated hydrocarbon such as dichloromethane, chloroform, 1,2-dichloroethane or the like; an aliphatic hydrocarbon such as pentane, hexane, cyclohexane, heptane or the like; a ketone such as acetone, methyl ethyl ketone, cyclohexanone or the like; water; and a mixed solvent thereof. Incidentally, the use amount of the solvent is 0.1 to 100 liters, preferably 0.3 to 10 liters relative to 1 mol of the compound [XXI].

The amount of the nitric acid used in the present step is appropriately selected in a range of 1.0 to 40 mols and is preferably 1.0 to 10 mols relative to 1 mol of the compound [XXI]. The amount of sulfuric acid when used is appropriately selected in a range of 1 to 40 mols and is preferably 1.0 to 10 mols relative to 1.0 mol of the compound [XXI].

The reaction temperature of the present step is freely selected in a range from 0° C. to the reflux temperature of the reaction system and is preferably 0° C. to 150° C.

The reaction time of the present step differs depending upon the temperature of reaction, the substrate of reaction, the amount of reactant, etc., but is ordinarily 10 minutes to 24 hours.

After the completion of the reaction, the reaction mixture is subjected to operations such as pouring into water or the like, extraction with organic solvent, concentration and the like, whereby a compound [XXII] can be isolated. The isolated compound [XXII] may be as necessary purified by column chromatography, recrystallization, etc.

[Step 7]

The compound represented by the general formula [XV] can be produced by reacting the compound [XXII] with iron/acid, zinc/acid, tin/acid, tin dichloride/acid, nickel chloride/sodium tetrahydroborate, lithium aluminum hydride, palladium-activated carbon/hydrogen, or the like, for reduction.

As the acid usable in the present step, there can be mentioned a mineral acid such as hydrochloric acid, sulfuric acid or the like. The amount of the iron/acid, zinc/acid, tin/acid, tin dichloride/acid, nickel(II) chloride/sodium tetrahydroborate, lithium aluminum hydride, palladium-activated carbon/hydrogen, or the like, used in the present step is appropriately selected in a range of 1.0 to 5.0 mols and is preferably 1.0 to 2.0 mols relative to 1 mol of the compound [XXII].

The reaction temperature of the present step is freely selected in a range from 0° C. to the reflux temperature of the reaction system and is preferably 0° C. to 100° C.

The reaction time of the present step differs depending upon the temperature of reaction, the substrate of reaction, the amount of reactant, etc., but is ordinarily 10 minutes to 24 hours.

After the completion of the reaction, the reaction mixture is subjected to operations such as pouring into water or the like, extraction with organic solvent, concentration and the like, whereby a compound [XV] can be isolated. The isolated compound [XV] may be as necessary purified by column chromatography, recrystallization, etc.

<Production Method 4 of Intermediate>

A compound represented by the general formula [XXV] can be produced by the method of the reaction formulas shown in the following [step 8] and [step 9].

(In the above reaction formulas, Z² is a same or different C₁˜C₆ alkyl group; and R¹, R², R³, Y¹ and n each have the same meaning as given above.)

[Step 8]

A compound represented by the general formula [XXIV] can be produced by reacting a compound [XXIII] with a metal or an organometallic compound in an appropriate solvent and then reacting the reaction product with a boric acid ester.

As the solvent usable in the present step, there can be mentioned, for example, an ether such as diethyl ether, tetrahydrofuran, 1,4-dioxane or the like; an aromatic hydrocarbon such as benzene, toluene, xylene, chlorobenzene or the like; an aliphatic hydrocarbon such as pentane, hexane, cyclohexane, heptane or the like; a pyridine such as pyridine, picoline or the like; and a mixed solvent thereof. Incidentally, the use amount of the solvent is 0.1 to 100 liters, preferably 0.1 to 5.0 liters relative to 1 mol of the compound [XXIII].

As the metal usable in the present step, there can be mentioned lithium, magnesium, etc. The use amount of the metal is appropriately selected in a range of 1.0 to 3.0 mols and is preferably 1.0 to 1.2 mols relative to 1 mol of the compound [XXIII].

As the organometallic compound usable in the present step, there can be mentioned an alkyllithium such as n-butyllithium or the like. The use amount of the organometallic compound is appropriately selected in a range of 1.0 to 3.0 mols and is preferably 1.0 to 1.2 mols relative to 1 mol of the compound [XXIII].

The reaction temperature of the present step is freely selected in a range from −100° C. to the reflux temperature of the reaction system, and is preferably −60° C. to room temperature.

The reaction time of the present step differs depending upon the temperature of reaction, the substrate of reaction, the amount of reactant, etc., but is ordinarily 5 minutes to 12 hours.

After the completion of the reaction, the reaction mixture is subjected to operations such as pouring into water or the like, extraction with organic solvent, concentration and the like, whereby a compound [XXIV] can be isolated. The isolated compound [XXIV] may be as necessary purified by column chromatography, recrystallization, etc.

[Step 9]

The compound [XXV] can be produced by reacting the compound [XXIV] with an acid in an appropriate solvent.

As the solvent usable in the present step, there can be mentioned, for example, an ether such as diethyl ether, tetrahydrofuran, 1,4-dioxane or the like; an aromatic hydrocarbon such as benzene, toluene, xylene, chlorobenzene or the like; an aprotic polar solvent such as N,N-dimethylformamide, N,N-dimethylacetamide, N-methyl-2-pyrrolidone, dimethyl sulfoxide, sulfolane or the like; an alcohol such as methanol, ethanol, 2-propanol or the like; a halogenated hydrocarbon such as dichloromethane, chloroform, dichloroethane or the like; an aliphatic hydrocarbon such as pentane, hexane, cyclohexane, heptane or the like; a ketone such as acetone, methyl ethyl ketone, cyclohexanone or the like; water; and a mixed solvent thereof. Incidentally, the use amount of the solvent is 0.1 to 100 liters, preferably 0.1 to 5.0 liters relative to 1 mol of the compound [XXIV].

As the acid usable in the present step, there can be mentioned a mineral acid such as sulfuric acid, hydrochloric acid or the like. The use amount of the acid is appropriately selected in a range of 1.0 to 5.0 mols and is preferably 0.5 to 2.0 mols relative to 1 mol of the compound [XXIV].

The reaction temperature of the present step is freely selected in a range from 0° C. to the reflux temperature of the reaction system and is preferably 0° C. to 100° C.

The reaction time of the present step differs depending upon the temperature of reaction, the substrate of reaction, the amount of reactant, etc., but is ordinarily 10 minutes to 24 hours.

After the completion of the reaction, the reaction mixture is subjected to operations such as pouring into water or the like, extraction with organic solvent, concentration and the like, whereby a compound [XXV] can be isolated. The isolated compound [XXV] may be as necessary purified by column chromatography, recrystallization, etc.

<Production Method 5 of Intermediate>

Of the compounds represented by the general formula [XV], a compound represented by [XV-1] can be produced by the method shown by the reaction formulas of the following [step 10] and [step 11].

(In the above reaction formulas, R¹, R², R³, Z² and L¹ each have the same meaning as given above.)

[Step 10]

A compound represented by the general formula [XXVII] can be produced by reacting a compound [XXVI] with chlorosulfonic acid, then reducing the reaction product with lithium aluminum hydride, zinc/acid, tin/acid, or red phosphorus/iodine, thereafter hydrolyzing the reaction product with a base.

As the acid usable in the present step, there can be mentioned a mineral acid such as hydrochloric acid, sulfuric acid or the like. The use amount of chlorosulfonic acid in the present step is appropriately selected in a range of 2.0 to 10 mols and is preferably 2.2 to 3.5 mols relative to 1 mol of the compound [XXVI].

The use amount of the lithium aluminum hydride, zinc/acid, tin/acid, or red phosphorus/iodine, in the present step is appropriately selected in a range of 1.0 to 5.0 mols and is preferably 1.5 to 2.0 mols relative to 1 mol of the compound [XXVI].

As the base usable in the present step, there can be mentioned sodium hydroxide, potassium hydroxide or the like. The use amount of the base is appropriately selected in a range of 1 to 5 mols and is preferably 1.0 to 3.0 mols relative to 1 mol of the compound [XXVI].

The reaction temperature of the present step is freely selected in a range from 0° C. to the reflux temperature of the reaction system and is preferably 0° C. to 100° C.

The reaction time of the present step differs depending upon the temperature of reaction, the substrate of reaction, the amount of reactant, etc., but is ordinarily 10 minutes to 24 hours.

After the completion of the reaction, the reaction mixture is subjected to operations such as pouring into water or the like, extraction with organic solvent, concentration and the like, whereby a compound [XXVII] can be isolated. The isolated compound [XXVII] may be as necessary purified by column chromatography, recrystallization, etc.

[Step 11]

The compound represented by the general formula [XV-1] can be produced by reacting the compound [XXVII] with a compound [III] in a solvent in the presence or absence of a base in the presence or absence of a radical initiator, in the same manner as in the Production method 1.

Each amount of the solvent and the base, usable in the present step is the same as in the Production method 1, and the reaction time and the reaction temperature in the present step are each the same as in the Production method 1.

After the completion of the reaction, the reaction mixture is subjected to operations such as pouring into water or the like, extraction with organic solvent, concentration and the like, whereby a compound [XV-1] can be isolated. The isolated compound [XV-1] may be as necessary purified by column chromatography, recrystallization, etc.

The pest control agent of the present invention is characterized by containing, as an active ingredient, an alkyl phenyl sulfide derivative represented by the general formulas [I] or [I′], or an agriculturally acceptable salt thereof. The present pest control agent is representatively an insecticide and miticide.

The present pest control agent may as necessary contain an additive component (carrier) ordinarily used in agricultural chemical formulations.

As the additive component, there can be mentioned a carrier (e.g. solid carrier or liquid carrier), a surfactant, a binder or a tackifier, a thickening agent, a coloring agent, a spreader, a sticker, an anti-freeze, a solidification inhibitor, a disintegrator, a decomposition inhibitor, etc. As necessary, there may be used other additive components such as antiseptic, vegetable chip and the like. These additive components may be used in one kind or in combination of two or more kinds.

The above additive components are explained.

As the solid carrier, there can be mentioned, for example, mineral carriers such as pyrophyllite clay, kaolin clay, silicastone clay, talc, diatomaceous earth, zeolite, bentonite, acid clay, active clay, Attapulgus clay, vermiculite, perlite, pumice, white carbon (e.g. synthetic silicic acid or synthetic silicate), titanium dioxide and the like; vegetable carriers such as wood flour, corn culm, walnut shell, fruit stone, rice hull, sawdust, wheat bran, soybean flour, powder cellulose, starch, dextrin, saccharide and the like; inorganic salt carriers such as calcium carbonate, ammonium sulfate, sodium sulfate, potassium chloride and the like; and polymer carriers such as polyethylene, polypropylene, polyvinyl chloride, polyvinyl acetate, ethylene-vinyl acetate copolymer, urea-aldehyde resin and the like.

As the liquid carrier, there can be mentioned, for example, monohydric alcohols such as methanol, ethanol, propanol, isopropanol, butanol, cyclohexanol and the like; polyhydric alcohols such as ethylene glycol, diethylene glycol, propylene glycol, hexylene glycol, polyethylene glycol, polypropylene glycol, glycerine and the like; polyhydric alcohol derivatives such as propylene type glycol ether and the like; ketones such as acetone, methyl ethyl ketone, methyl isobutyl ketone, diisobutyl ketone, cyclohexanone, isophorone and the like; ethers such as diethyl ether, 1,4-dioxane, cellosolve, dipropyl ether, tetrahydrofuran and the like; aliphatic hydrocarbons such as normal paraffin, naphthene, isoparaffin, kerosene, mineral oil and the like; aromatic hydrocarbons such as toluene, C₉˜C₁₀ alkylbenzene, xylene, solvent naphtha, alkylnaphthalene, high-boiling aromatic hydrocarbon and the like; halogenated hydrocarbons such as 1,2-dichloroethane, chloroform, carbon tetrachloride and the like; esters such as ethyl acetate, diisopropyl phthalate, dibutyl phthalate, dioctyl phthalate, dimethyl adipate and the like; lactones such as γ-butyrolactone and the like; amides such as dimethylformamide, diethylformamide, dimethylacetamide, N-alkylpyrrolidinone and the like; nitriles such as acetonitrile and the like; sulfur compounds such as dimethyl sulfoxide and the like; vegetable oils such as soybean oil, rapeseed oil, cottonseed oil, coconut oil, castor oil and the like; and water.

As to the surfactant, there is no particular restriction. However, the surfactant preferably gels or swells in water. There can be mentioned, for example, non-ionic surfactants such as sorbitan fatty acid ester, polyoxyethylene sorbitan fatty acid ester, sucrose fatty acid ester, polyoxyethylene fatty acid ester, polyoxyethylene resin acid ester, polyoxyethylene fatty acid diester, polyoxyethylene alkyl ether, polyoxyethylene alkylphenyl ether, polyoxyethylene dialkylphenyl ether, polyoxyethylene alkylphenyl etherformalin condensate, polyoxyethylene polyoxypropylene block polymer, alkyl polyoxyethylene polypropylene block polymer ether, polyoxyethylene alkyl amine, polyoxyethylene fatty acid amide, polyoxyethylene fatty acid bisphenyl ether, polyalkylene benzyl phenyl ether, polyoxyalkylene styryl phenyl ether, acetylene diol, polyoxyalkylene-added acetylene diol, polyoxyethylene ether type silicone, ester type silicone, fluorine-containing surfactant, polyoxyethylene castor oil, polyoxyethylene hardened castor oil and the like; anionic surfactants such as alkyl sulfate, polyoxyethylene alkyl ether sulfate, polyoxyethylene alkyl phenyl ether sulfate, polyoxyethylene styryl phenyl ether sulfate, alkylbenzenesulfonic acid salt, ligninsulfonic acid salt, alkylsulfosuccinic acid salt, naphthalenesulfonic acid salt, alkylnaphthalenesulfonic acid salt, naphthalenesulfonic acid-formalin condensate salt, alkylnaphthalenesulfonic acid-formalin condensate salt, fatty acid salt, polycarboxylic acid salt, N-methyl-fatty acid sarcosinate, resin acid salt, polyoxyethylene alkyl ether phosphate, polyoxyethylene alkylphenyl ether phosphate and the like; cationic surfactants including alkyl amine salts such as laurylamine hydrochloride, stearylamine hydrochloride, oleylamine hydrochloride, stearylamine acetate, stearylaminopropylamine acetate, alkyl trimethyl ammonium chloride, alkyl dimethyl benzalkonium chloride and the like; and ampholytic surfactants such as betaine type (e.g. dialkyldiaminoethylbetaine or alkyldimethylbenzylbetaine), amino acid type (e.g. dialkylaminoethylglycine or alkyldimethylbenzylglycine) and the like.

As the binder and tackifier, there can be mentioned, for example, carboxymethyl cellulose or a salt thereof, dextrin, water-soluble starch, xanthane gum, guar gum, sucrose, polyvinylpyrrolidone, gum arabi, polyvinyl alcohol, polyvinyl acetate, sodium polyacrylate, polyethylene glycol having an average molecular weight of 6,000 to 20,000, polyethylene oxide having an average molecular weight of 100,000 to 5,000,000, and natural phospholipid (e.g. cephalinic acid or lecithin).

As the thickening agent, there can be mentioned, for example, water-soluble polymers such as xanthan gum, guar gum, carboxymethyl cellulose, polyvinylpyrrolidone, carboxyvinyl polymer, acrylic polymer, starch derivative, polysaccharide and the like; and inorganic fine powders such as high-purity bentonite, white carbon and the like.

As the coloring agent, there can be mentioned, for example, inorganic pigments such as iron oxide, titanium oxide, Prussian Blue and the like; and organic dyes such as Alizarine dye, azo dye, metal phthalocyanine dye and the like.

As the spreader, there can be mentioned, for example, silicone-based surfactant, cellulose powder, dextrin, processed starch, polyaminocarboxylic acid chelate compound, crosslinked polyvinylpyrrolidone, maleic acid and styrene, methacrylic acid copolymer, half ester between polyhydric alcohol polymer and dicarboxylic acid anhydride, and water-soluble salt of polystyrenesulfonic acid.

As the sticker, there can be mentioned, for example, surfactant (e.g. sodium dialkylsulfosuccinate, polyoxyethylene alkyl ether, polyoxyethylene alkylphenyl ether, or polyoxyethylene fatty acid ester), paraffin, terpene, polyamide resin, polyacrylic acid salt, polyoxyethylene, wax, polyvinyl alkyl ether, alkylphenol-formalin condensate, and synthetic resin emulsion.

As the anti-freeze, there can be mentioned, for example, polyhydric alcohol (e.g. ethylene glycol, diethylene glycol, propylene glycol, or glycerine).

As the solidification inhibitor, there can be mentioned, for example, polysaccharide (e.g. starch, alginic acid, mannonse or galactose), polyvinylpyrrolidone, white carbon, ester gum and petroleum resin.

As the disintegrator, there can be mentioned, for example, sodium tripolyphosphate, sodium hexametaphosphate, stearic acid metal salt, cellulose powder, dextrin, methacrylic acid ester copolymer, polyvinylpyrrolidone, polyaminocarboxylic acid chelate compound, sulfonated styrene-isobutylene-maleic anhydride copolymer, and starch-polyacrylonitrile graft copolymer.

As the decomposition inhibitor, there can be mentioned, for example, desiccants such as zeolite, quick lime, magnesium oxide and the like; antioxidants such as phenol type, amine type, sulfur type, phosphoric acid type and the like; and ultraviolet absorbents such as salicylic acid type, benzophenone type and the like.

When the present pest control agent contains the above-mentioned additive components, their contents based on mass are selected in a range of ordinarily 5 to 95%, preferably 20 to 90% in the case of carrier (e.g. solid carrier or liquid carrier), ordinarily 0.1 to 30%, preferably 0.5 to 10% in the case of surfactant, and ordinarily 0.1 to 30%, preferably 0.5 to 10% in the case of other additives.

The present pest control agent is used in any formulation selected from dust formulation, dust-granule mixture, granule, wettable powder, water-soluble concentrate, water-dispersible granule, tablet, Jumbo, emulsifiable concentrate, oil formulation, solution, flowable concentrate, emulsion, microemulsion, suspoemulsion, ultra-low volume formulation, microcapsule, smoking agent, aerosol, baiting agent, paste, etc.

In actual use of the formulation, the formulation can be used per se or after dilution with a diluent (e.g. water) in a given concentration. The application of the formulation containing the present compound or of its dilution product can be conducted by a method ordinarily used, such as dispersion (e.g. spraying, misting, atomizing, powder dispersion, granule dispersion, on-water-surface dispersion, or inbox dispersion), in-soil application (e.g. mixing or drenching), on-surface application (e.g. coating, dust coating or covering), immersion, poison bait, smoking and the like. It is also possible to mix the above-mentioned active ingredient with a livestock feed in order to prevent the infestation and growth of injurious pest, particularly injurious insect in the excreta of livestock.

The proportion (mass %) of the active ingredient in the present pest control agent is appropriately selected so as to meet the necessity. The active ingredient is appropriately selected, for example, in the following range.

In dust formulation, dust-granule mixture, etc.

0.01 to 20%, preferably 0.05 to 10%

In granule, etc.

0.1 to 30%, preferably 0.5 to 20%

In wettable powder, water-dispersible granule, etc.

1 to 70%, preferably 5 to 50%

In water-soluble concentrate, solution, etc

1-95%, preferably 10 to 80%

In emulsifiable concentrate, etc.

5 to 90%, preferably 10 to 80%

In oil formulation, etc.

1 to 50%, preferably 5 to 30%

In flowable concentrate, etc.

5 to 60%, preferably 10 to 50%

In emulsion, microemulsion, suspoemulsion, etc.

5 to 70%, preferably 10 to 60%

In tablet, bait, paste, etc.

1 to 80%, preferably 5 to 50%

In smoking agent, etc.

0.1 to 50%, preferably 1 to 30%

In aerosol, etc.

0.05 to 20%, preferably 0.1 to 10%

The formulation is sprayed after dilution in an appropriate concentration, or applied directly.

When the present pest control agent is used after dilution with a diluent, the concentration of active ingredient is generally 0.1 to 5,000 ppm. When the formulation is used per se, the application amount thereof per unit area is 0.1 to 5,000 g per 1 ha in terms of active ingredient compound; however, the application amount is not restricted thereto.

Incidentally, the present pest control agent is sufficiently effective when using the present compound alone as an active ingredient. However, in the present pest control agent, there may be mixed or used in combination, as necessary, fertilizers and agricultural chemicals such as insecticide, miticide, nematicide, synergist, fungicide, antiviral agent, attractant, herbicide, plant growth-controlling agent and the like. In this case, a higher effect is exhibited.

Below are shown examples of the known insecticides, miticides, nematicides and synergist compounds, which may be mixed or used in combination.

1. Acetylcholinesterase Inhibitors

(1A) carbamates: alanycarb, aldicarb, aldoxycarb, bendiocarb, benfuracarb, butocarboxim, butoxycarboxim, carbaryl, carbofuran, carbosulfan, ethiofencarb, fenobucarb, formetanate, furathiocarb, isoprocarb, methiocarb, methomyl, metolcarb, oxamyl, pirimicarb, propoxur, thiodicarb, thiofanox, triazamate, trimethacarb, XMC, xylylcarb;

(1B) Organophosphates: acephate, azamethiphos, azinphosethyl, azinphos-methyl, cadusafos, chlorethoxyfos, chlorfenvinphos, chlormephos, chlorpyrifos, chlorpyrifos-methyl, coumaphos, cyanophos, demoton-S-methyl, diamidafos, diazinon, dichlorvos, dicrotophos, dimethoate, dimethylvinphos, dioxabenzofos, disulfoton, DSP, EPN, ethion, ethoprophos, etrimfos, famphur, fenamiphos, fenitrothion, fenthion, fonofos, fosthiazate, fosthietan, heptenophos, isamidofos, isazophos, isofenphos-methyl, isopropyl O-(methoxyaminothiophosphoryl)salicylate, isoxathion, malathion, mecarbam, methamidophos, methidathion, mevinphos, monocrotophos, naled, omethoate, oxydemeton-methyl, oxydeprofos, parathion, parathion-methyl, phenthoate, phorate, phosalone, phosmet, phosphamidon, phoxim, pirimiphos-methyl, profenofos, propaphos, propetamphos, prothiofos, pyraclofos, pyridaphenthion, quinalphos, sulfotep, tebupirimfos, temephos, terbufos, tetrachlorvinphos, thiometon, thionazin, triazophos, trichlorfon, vamidothion, dichlofenthion, imicyafos, isocarbophos, mesulfenfos, flupyrazofos

2. GABA-Gated Chloride Channel Antagonists

(2A) Cyclodiene organochlorines: chlordane, endosulfan, gamma-BCH;

(2B) Phenylpyrazoles: acetoprol, ethiprole, fipronil, pyrafluprole, pyriprole, RZI-02-003 (code number)

3. Sodium Channel Modulators

(3A) Pyrethroids/Pyrethrins: acrinathrin, allethrin (includes d-cis-trans and d-trans), bifenthrin, bioallethrin, bioallethrin S-cyclopentenyl, bioresmethrin, cycloprothrin, cyfluthrin (includes beta-), cyhalothrin (includes gamma- and lambda-), cypermethrin (includes alpha-, beta-, theta- and zeta-), cyphenothrin [includes (IR)-trans-isomers], deltamethrin, empenthrin, esfenvalerate, etofenprox, fenpropathrin, fenvalerate, flucythrinate, flumethrin, halfenprox, imiprothrin, metofluthrin, permethrin, phenothrin [includes (IR)trans-isomer], prallethrin, profluthrin, pyrethrine, resmethrin, RU15525 (code number), silafluofen, tefluthrin, tetramethrin, tralomethrin, transfluthrin, ZX18901 (code number), fluvalinate (includes tau-), tetramethylfluthrin, meperfluthrin;

(3B) DDT/Methoxychlor: DDT, methoxychlor

4. Nicotinic Acetylcholine Receptor Agonist/Antagonist

(4A) Neonicotinoids: acetamiprid, clothianidin, dinotefuran, imidacloprid, nitenpyram, thiacloprid, thiamethoxam;

(4B) Nicotine: nicotine-sulfate

5. Nicotinic Acetylcholine Receptor Allosteric Activators

Spinosines: spinetoram, spinosad

6. Chloride Channel Activators

Abamectins, Milbemycins: abamectin, emamectin benzoate, lepimectin, milbemectin, ivermectin, polynactins

7. Juvenile Hormone Mimics

diofenolan, hydroprene, kinoprene, methothrin, fenoxycarb, pyriproxyfen

8. Miscellaneous Non-Specific (Multi-Site) Inhibitors

1,3-dichloropropene, DCIP, ethylene dibromide, methyl bromide, chloropicrin, sulfuryl fluoride

9. Antifeedant

pymetrozine, flonicamid, pyrifluquinazon

10. Mite Growth Inhibitor

clofentezine, diflovidazin, hexythiazox, etoxazole

11. Microbial Disruptors of Insect Midgut Membranes

BT agent: Bacillus sphaericus, Bacillus thuringiensis subsp. aizawai, Bacillus thuringiensis subsp. israelensis, Bacillus thuringiensis subsp. kurstaki, Bacillus thuringiensis subsp. tenebrionis, Bt crop proteins (Cry1Ab, Cry1Ac, Cry1Fa, Cry2Ab, mCry3A, Cry3Ab, Cry3Bb, Cry34/35Ab1), Bacillus popilliae, Bacillus subtillis

12. Inhibitors of Mitochondrial ATP Synthase Diafenthiuron;

Organotin miticides: azocyclotin, cyhexatin, fenbutatin oxide;

propargite, tetradifon

13. Uncouplers of Oxidative Phosphorylation Via Disruption of the Proton Gradient

chlorfenapyr, DNOC

14. Nicotinic Acetylcholine Receptor Channel Blockers

Nereistoxin analogues: bensultap, cartap, thiocyclam, thiosultap

15. Inhibitors of Chitin Biosynthesis, Type O

Benzoylureas: bistrifluron, chlorfluazoron, diflubenzuron, flucycloxuron, flufenoxuron, hexaflumuron, lufenuron, novaluron, noviflumuron, teflubenzuron, triflumuron, fluazuron

16. Inhibitors of Chitin Biosynthesis, Type 1

buprofezin

17. Molting Disruptor, Dipteran

cyromazine

18. Ecdysone Receptor Agonist (Ecdysis Acceleration)

Diacylhydrazines: chromafenozide, halofenozide, methoxyfenozide, tebufenozide

19. Octopamine Receptor Agonist

amitraz

20. Mitochondrial Complex III Electron Transport Inhibitors

hydramethylnon, acequinocyl, fluacrypyrim, cyenopyrafen

21. Mitochondrial Complex II Electron Transport Inhibitors

cyflumetofen, cyenopyrafen, NNI-0711 (code number)

22. Mitochondrial Complex I Electron Transport Inhibitors

METI miticides and insecticides: fenazaquin, fenpyroximate, pyridaben, pyrimidifen, tebufenpyrad, tolfenpyrad

Other: rotenone

23. Sodium Channel Blockers

indoxacarb, metaflumizon

24. Inhibitors of Lipid Synthesis

Tetronic and Tetramic acid derivatives: spirodiclofen, spiromesifen, spirotetramat

25. Mitochondrial Complex IV Electron Transport Inhibitors

aluminum phosphide, phosphine, zinc phosphide, calcium cyanide

26. Neuronal Inhibitors (Unknown Mode of Action)

bifenazate

27. Aconitase Inhibitors

sodium fluoroacetate

28. Synergists

piperonyl butoxide, DEF

29. Ryanodine Receptor Modulators

chlorantraniliprole, flubendiamide, cyantraniliprole

30. Compounds with Unknown Mode of Action

azadirachtin, amidoflumet, benclothiaz, benzoximate, bromopropylate, chinomethionat, CL900167 (code number), cryolite, dicofol, dicyclanil, dienochlor, dinobuton, fenbutatin oxide, fenothiocarb, fluensulfone, flufenerim, flsulfamide, karanjin, metham, methoprene, methoxyfenozide, methyl isothiocyanate, pyridalyl, pyrifluquinazon, sulcofuron-sodium, sulfluramid, sulfoxaflor, flupyradifurone, flometoquin, IKI-3106 (code number)

31. Entomopathogenic Fungi, Nematode-Pathogenic Microorganisms

Beauveria bassiana, Beauveria tenella, Verticillium lecanii, Pacilimyces tenuipes, Paecilomyces fumosoroceus, Beauveria brongniartii, Monacrosporium phymatophagum, Pasteuriapenetrans

32. Sex Pheromone

(Z)-11-hexadecenal, (Z)-11-hexadecenyl acetate, litlure-A, litlure-B, Z-13-eicosene-10-one, (Z,E)-9,12-tetradecadienyl acetate, (Z)-9-tetradecen-1-ol, (Z)-11-tetradecenyl acetate, (Z)-9,12-tetradecadienyl acetate, (Z,E)-9,11-detradecadienyl acetate

Next, there are shown examples of the known fungicide or disease damage control agent compounds which may be mixed or used in combination.

1. Nucleic Acid Biosynthesis Inhibitor

Acylalanines: benalaxyl, benalaxyl-M, furalaxyl, metalaxyl, metalaxyl-M;

Oxazolidinones: oxadixyl;

Butyrolactones: clozylacon, ofurace;

Hydroxy-(2-amino)pyrimidines: bupirimate, dimethirimol, ethirimol;

Isoxazole: hymexazol;

Isothiazolones: octhilinone;

Carboxylic acids: oxolinic acid

2. Mitosis and Cell Division Inhibitors

Benzoimidazoles: benomyl, carbendazim, fuberidazole, thiabendazole;

Thiophanates: thiophanate, thiophanate-methyl;

N-phenylcarbamates: diethofencarb;

Toluamides: zoxamide;

Phenylureas: pencycuron;

Pyridinylmethylbenzamides: fluopicolide

3. Respiratory Inhibitors

Pyrimidineamines: diflumetorim;

Carboxamides: benodanil, flutolanil, mepronil, fluopyram, fenfuram, carboxin, oxycarboxin, thifluzamide, bixafen, furametpyr, isopyrazam, penflufen, penthiopyrad, sedaxane, boscalid, fluxapyroxad, isofetamid, benzovindiflupyr;

Methoxy-acrylates: azoxystrobin, enestroburin, picoxystrobin, pyraoxystrobin, coumoxystrobin, enoxastrobin, flufenoxystrobin;

Methoxy-carbamates: pyraclostrobin, pyrametostrobin, triclopyricarb;

Oxyimino acetates: kresoxim-methyl, trifloxystrobin;

Oxyimino-acetamides: dimoxystrobin, metominostrobin, orysastrobin, fenaminstrobin;

Oxazolidine-diones: famoxadone;

Dihydro-dioxazines: fluoxastrobin;

Imidazolinones: fenamidone;

Benzyl-carbamates: pyribencarb;

Cyano-imidazoles: cyazofamid;

Sulfamoyl-triazoles: amisulbrom;

Dinitrophenyl crotonates: binapacryl, methyldinocap, dinocap;

2,6-Dinitro-anilines: fluazinam;

Pyrimidinone hydrazones: ferimzone;

Triphenyl tin: TPTA, TPTC, TPTH;

Thiophene-carboxamides: silthiofam

Triazolo-pyrimidylamines: ametoctradin

4. Amino Acid and Protein Synthesis Inhibitors

Anilino-pyrimidines: cyprodinil, mepanipyrim, pyrimethanil;

Enopyranuronic acid: blasticidin-S, mildiomycin;

Hexopyranosyl antibiotic: kasugamycin;

Glucopyranosyl antibiotic: streptomycin;

Tetracycline antibiotic: oxytetracycline

5. Signal Transduction Inhibitors

Quinoline: quinoxyfen;

Quinazolines: proquinazid;

Phenylpyrroles: fenpiclonil, fludioxonil;

Dicarboxyimides: chlozolinate, iprodione, procymidone, vinclozolin

6. Lipid Synthesis and Membrane Integrity Inhibitors

Phosphoro-thiolates: edifenphos, iprobenfos, pyrazophos;

Dithiolanes: isoprothiolane;

Aromatic hydrocarbons: biphenyl, chloroneb, dicloran, quintozene, tecnazene, tolclofos-methyl;

1,2,4-Thiadiazoles: etridiazole;

Carbamates: iodocarb, propamocarb-hydrochloride, prothiocarb;

Cinnamic acid amides: dimethomorph, flumorph;

Valineamide carbamates: benthiavalicarb-isopropyl, iprovalicarb, valifenalate;

Mandelic acid amides: mandipropamid;

Bacillus subtilis and the fungicidal lipopeptides produced: Bacillus subtilis (strain: QST 713)

7. Inhibitors of Sterol Biosynthesis in Membranes

Piperazines: triforine;

Pyridines: pyrifenox;

Pyrimidines: fenarimol, nuarimol;

Imidazoles: imazalil, oxpoconazole-fumarate, pefurazoate, prochloraz, triflumizole;

Triazoles: azaconazole, bitertanol, bromuconazole, cyproconazole, difenoconazole, diniconazole, diniconazole-M, epoxiconazole, etaconazole, fenbuconazole, fluquinconazole, flusilazole, flutriafol, hexaconazole, imibenconazole, ipconazole, metconazole, myclobutanil, penconazole, propiconazole, prothioconazole, simeconazole, tebuconazole, tetraconazole, triadimefon, triadimenol, triticonazole, furconazole, furconazole-cis, quinconazole;

Morpholines: aldimorph, dodemorph, fenpropimorph, tridemorph;

Piperidines: fenpropidin, piperalin;

Spiroketal amines: spiroxamine;

Hydroxyanilides: fenhexamid;

Thiocarbamates: pyributicarb;

Allylamines: naftifine, terbinafine

8. Glucan Synthesis Inhibitors

Glucopyranosyl type antibiotic: validamycin;

Peptidylpyridine nucleotide compound: polyoxin

9. Melanine Synthesis Inhibitors

Isobenzo-furanones: phthalide;

Pyrrolo-quinolines: pyroquilon;

Triazolobenzo-thiazoles: tricyclazole;

Carboxamides: carpropamid, diclocymet;

Propionamides: fenoxanil

10. Host Plant Defense Inducers

Benzothiadiazoles: acibenzolar-S-methyl;

Benzoisothiazoles: probenazole;

Thiadiazole-carboxamides: tiadinil, isotianil

Natural product: laminarin

11. Compounds with Unknown Mode of Action

Copper compound: copper hydroxide, copper dioctanoate, copper oxychloride, copper sulfate, cuprous oxide, oxinecopper, Bordeaux mixture, copper nonyl phenol sulphonate;

Sulfur compound: sulfur;

Dithiocarbamates: ferbam, mancozeb, maneb, metiram, propineb, thiram, zineb, ziram, cufraneb;

Phthalimides: captan, folpet, captafol;

Chloronitriles: chlorothalonil;

Sulfamides: dichlofluanid, tolylfluanid;

Guanidines: guazatine, iminoctadine-albesilate, iminoctadine-triacetate, dodine;

Other compound: anilazine, dithianon, cymoxanil, fosetyl (alminium, calcium, sodium), phosphorus acid and salts, tecloftalam, triazoxide, flusulfamide, diclomezine, methasulfocarb, ethaboxam, cyflufenamid, metrafenone, potassium bicarbonate, sodium bicarbonate, BAF-045 (code number), BAG-010 (code number), benthiazole, bronopol, carvone, chinomethionat, dazomet, DBEDC, debacarb, dichlorophen, difenzoquat-methyl sulfate, dimethyl disulfide, diphenylamine, ethoxyquin, flumetover, fluoroimide, flutianil, furancarboxylic acid, metam, nabam, natamycin, nitrapyrin, nitrothal-isopropyl, ophenylphenol, oxazinylazole, oxyquinoline sulfate, phenazine oxide, polycarbamate, pyriofenone, fenpyrazamine, silver, pyrisoxazole, tebufloquin, tolnifanide, trichlamide, mineral oils, organic oils, tolprocarb, oxathiapiprolin

Below are shown examples of the known herbicidal compounds and plant growth regulators which may be mixed or used in combination.

A1. Acetyl CoA Carboxylase (ACCase) Inhibitors

(A1-1) Aryloxyphenoxy propionates: clodinafop-propargyl, cyhalofop-butyl, diclofop-methyl, diclofop-P-methyl, fenoxaprop-P-ethyl, fluazifop-butyl, fluazifop-P-butyl, haloxyfop, haloxyfop-etotyl, haloxyfop-P, metamifop, propaquizafop, quizalofop-ethyl, quizalofop-P-ethyl, quizalofop-P-tefuryl, fenthiaprop-ethyl; (A1-2) Cyclohexandiones: alloxydim, butroxydim, clethodim, cycloxydim, profoxydim, sethoxydim, tepraloxydim, tralkoxydim; (A1-3) Phenylpyrazolines: aminopyralid, pinoxaden;

B. Acetolactate Synthase (ALS) Inhibitors

(B-1) Imidazolinones: imazamethabenz-methyl, imazamox, imazapic (includes salts with amine, etc.), imazapyr (includes salts with isopropylamine, etc.), imazaquin, imazathapyr; (B-2) Pyrimidinyloxy benzoate: bispyribac-sodium, pyribenzoxim, pyriftalid, pyriminobac-methyl, pyrithiobac-sodium, pyrimisulfan, triafamone; (B-3) Sulfonylaminocarbonyl-triazolinones: flucarbazonesodium, thiencarbazone (includes sodium salt, methyl ester, etc.), propoxycarbazone-sodium, procarbazone-sodium, iofensulfuron-sodium; (B-4) Sulfonylureas: amidosulfuron, azimsulfuron, bensulfuron-methyl, chlorimuron-ethyl, chlorsulfuron, cinosulfuron, cyclosulfamuron, ethametsulfuron-methyl, ethoxysulfuron, flazasulfuron, flupyrsulfuron-methyl-sodium, foramsulfuron, halosulfuron-methyl, imazosulfuron, iodosulfulon-methyl-sodium, mesosulfuron-methyl, thifensulfuron-methyl, triasulfuron, tribenuron-methyl, trifloxysulfuron-sodium, triflusulfuron-methyl, tritosulfuron, orthosulfamuron, propgirisulfuron, metazosulfuron, flucetosulfuron; (B-5) Triazolopyrimidines: cloransulam-methyl, diclosulam, florasulam, flumetsulam, metosulam, penoxsulam, pyroxsulam;

C1. Photosynthesis at Photosystem II Inhibitors (1)

(C1-1) Phenylcarbamates: desmedipham, phenmedipham; (C1-2) Pyridazinones: chloridazon, brompyrazon; (C1-3) Triazines: ametryn, atrazine, cyanazine, desmetryne, dimethametryn, eglinazine-ethyl, prometon, prometryn, propazine, simazine, simetryn, terbumeton, terbuthylazine, terbutryn, trietazine; (C1-4) Triazinones: metamitron, metribuzin; (C1-5) Triazolinones: amicarbazone; (C1-6) Uracils: bromacil, lenacil, terbacil;

C2. Photosynthesis at Photosystem II Inhibitors (2)

(C2-1) Amides: pentanochlor, propanil; (C2-2) Ureas: chlorbromuron, chlorotoluron, chloroxuron, dimefuron, diuron, ethidimuron, fenuron, fluometuron, isoproturon, isouron, linuron, methabenzthiazuron, metobromuron, metoxuron, monolinuron, neburon, siduron, tebuthiuron, metobenzuron;

C3. Photosynthesis at Photosystem II Inhibitors (3)

(C3-1) Benzothiadiazones: bentazone; (C3-2) Nitriles: bromofenoxim, bromoxynil (includes esters of butyric acid, octanoic acid, heptanoic acid, etc.), ioxynil; (C3-3) Phenylpyrazines: pyridafol, pyridate;

D. Photosystem-I-Electron Acceptors

(D-1) Bipyridyliums: diquat, paraquat dichloride;

E. Protoporphyrinogen Oxydaze (PPO) Inhibitors

(E-1) Diphenylethers: acifluorfen-sodium, bifenox, chlomethoxyfen, ethoxyfen-ethyl, fluoroglycofen-ethyl, fomesafen, lactofen, oxyfluorfen; (E-2) N-phenylphthalimides: cinidon-ethyl, flumiclorac-pentyl, flumioxazin, chlorphthalim; (E-3) Oxydiazoles: oxadiargyl, oxadiazon; (E-4) Oxazolidinediones: pentoxazone; (E-5) Phenylpyrazoles: fluazolate, pyraflufen-ethyl; (E-6) Pyrimidinediones: benzfendizone, butafenacil, saflufenacil, tiafenacil; (E-7) Thiadiazoles: fluthiacet-methyl, thidiazimin; (E-8) Triazolinones: azafenidin, carfentrazone-ethyl, sulfentrazone, bencarbazone; (E-9) Other compound: flufenpyr-ethyl, profluazol, pyraclonil, SYP-298 (code number), SYP-300 (code number);

F1. Inhibitors of Carotenoid Biosynthesis at the Phytoene Desaturase Step (PDS)

(F1-1) Pyridazinones: norflurazon; (F1-2) Pyrimidinecarboxamides: diflufenican, picolinafen; (F1-3) Other compound: beflubutamid, fluridone, flurochloridone, flurtamone;

F2. 4-Hydroxyphenyl-Pyruvate-Dioxygenase (HPPD) Inhibitors

(F2-1) Callistemones: mesotrione; (F2-2) Isoxazoles: pyrasulfotole, isoxaflutole, isoxachlortole; (F2-3) Pyrazoles: benzofenap, pyrazolynate, pyrazoxyfen, topramezone; (F2-4) Triketones: sulcotrione, tefuryltrione, tembotrione, pyrasulfotole, topramezone, bicyclopyrone;

F3. Carotinoid Biosynthesis Inhibitors (Unknown Target)

(F3-1) Diphenyl ethers: aclonifen; (F3-2) Isoxazolidinones: clomazone; (F3-3) Triazoles: amitrole;

G. EPSP Synthase Inhibitors (Aromatic Amino Acid Biosynthesis Inhibitors)

(G-1) Glycines: glyphosate (includes salts of sodium, amine, propylamine, isopropylamine, dimethylamine, trimesium, etc.);

H. Glutamine Synthetase Inhibitors

(H-1) Phosphinic acids: bilanafos, glufosinate (includes salts of amine, sodium, etc.);

I. Dihydropteroate (DHP) Synthetase Inhibitors

(I-1) Carbamates: asulam;

K1. Microtubule Assembly Inhibitors

(K1-1) Benzamides: propyzamide, tebutam; (K1-2) Benzoic acids: chlorthal-dimethyl; (K1-3) Dinitroanilines: benfluralin, butralin, dinitramine, ethalfluralin, fluchloralin, oryzalin, pendimethalin, prodiamine, trifluralin; (K1-4) Phosphoroamidates: amiprofos-methyl, butamifos; (K1-5) Pyridines: dithiopyr, thiazopyr;

K2. Inhibitors of Mitosis/Microtubule Organization

(K2-1) Carbamates: carbetamide, chlorpropham, propham, swep, karbutilate;

K3. Very-Long-Chain Fatty Acids (VLCFAs) Inhibitors (Cell Division Inhibitors)

(K3-1) Acetamides: diphenamid, napropamide, naproanilide; (K3-2) Chloroacetamides: acetochlor, alachlor, butachlor, butenachlor, diethatyl-ethyl, dimethachlor, dimethenamid, dimethenamid-P, metazachlor, metolachlor, pethoxamid, pretilachlor, propachlor, propisochlor, S-metolachlor, thenylchlor; (K3-3) Oxyacetamides: flufenacet, mefenacet; (K3-4) Tetrazolinones: fentrazamide; (K3-5) Other compound: anilofos, bromobutide, cafenstrole, indanofan, piperophos, fenoxasulfone, pyroxasulfone, ipfencarbazone;

L. Cellulose Synthesis Inhibitors

(L-1) Benzamides: isoxaben; (L-2) Nitriles: dichlobenil, chlorthiamid; (L-3) Triazolocarboxamides: flupoxame;

M. Uncouplers (Membrane Disruptors)

(M-1) Dinitrophenols: dinoterb, DNOC (includes salts of amine, sodium, etc.);

N. Lipid Biosynthesis Inhibitors (Excluding ACCase Inhibitors)

(N-1) Benzofurans: benfuresate, ethofumesate; (N-2) Halogenated carboxylic acids: dalapon, flupropanate, TCA (includes salts of sodium, calcium, ammonia, etc.); (N-3) Phosphorodithioates: bensulide; (N-4) Thiocarbamates: butylate, cycloate, dimepiperate, EPIC, esprocarb, molinate, orbencarb, pebulate, prosulfocarb, thiobencarb, tiocarbazil, tri-allate, vernolate;

O. Synthetic Auxins

(O-1) Benzoic acids: chloramben, 2,3,6-TBA, dicamba (includes salts of amine, diethylamine, isopropylamine, diglycolamine, sodium, lithium, etc.); (O-2) Phenoxycarboxylic acids: 2,4,5-T, 2,4-D (includes salts of amine, diethylamine, triethanolamine, isopropylamine, sodium, lithium, etc.), 2,4-DB, clomeprop, dichlorprop, dichlorprop-P, MCPA, MCPA-thioethyl, MCPB (includes sodium salt, ethylester, etc.), mecoprop (includes salts of sodium, potassium, isopropylamine, triethanolamine, dimethylamine, etc.), mecoprop-P; (O-3) Pyridine carboxylic acids: clopyralid, fluroxypyr, picloram, triclopyr, triclopyr-butotyl, halauxifen-methyl; (O-4) Quinoline carboxylic acids: quinclorac, quinmerac; (O-5) Other compound: benazolin;

P. Auxin Transport Inhibitors

(P-1) Phthalamates: naptalam (includes salts with sodium, etc.); (P-2) Semicarbazones: diflufenzopyr; Z. Compounds with Unknown Mode of Action

flamprop-M (includes methyl, ethyl and isopropyl esters), flamprop (includes methyl, ethyl and isopropyl esters), chlorflurenol-methyl, cinmethylin, cumyluron, daimuron, methyldymuron, difenzoquat, etobenzanid, fosamine, pyributicarb, oxaziclomefone, acrolein, AE-F-150954 (code number), aminocyclopyrachlor, cyanamide, heptamaloxyloglucan, indaziflam, triaziflam, quinoclamine, endothal-disodium, phenisopham, SL573 (code number), cyclopyrimonate

Plant growth-controlling agent: 1-methylcyclopropene, 1-naphthylacetamide, 2,6-diisopropylnaphthalene, 4-CPA, benzylaminopurine, ancymidol, aviglycine, carvone, chlormequat, cloprop, cloxyfonac, cloxyfonac-potassium, cyclanilide, cytokinins, daminozide, dikegulac, dimethipin, ethephon, ethychlozate, flumetralin, flurenol, flurprimidol, forchlorfenuron, gibberellin acid, inabenfide, indole acetic acid, indole butyric acid, maleic hydrazide, mefluidide, mepiquat chloride, n-decanol, paclobutrazol, prohexadionecalcium, prohydrojasmon, sintofen, thidiazuron, triacontanol, trinexapac-ethyl, uniconazole, uniconazole-P, 4-oxo-4-(2-phenylethyl)aminobutyric acid (chemical name, CAS registration No.: 1083-55-2)

Next, there are shown examples of the known safners which may be mixed or used in combination.

benoxacor, furilazole, dichlormid, dicyclonone, DKA-24 (N1,N2-diallyl-N2-dichloroacetylglycineamide), AD-67 (4-dichloroacetyl-1-oxa-4-azaspiro[4.5]decane), PPG-1292 (2,2-dichloro-N-(1,3-dioxolan-2-ylmethyl)-N-(2-propenyl)acetamide), R-29148 (3-dichloroacetyl-2,2,5-trimethyl-1,3-oxazolidine), cloquintcet-methyl, 1,8-Naphthalic Anhydride, mefenpyrdiethyl, mefenpyr, mefenpyr-ethyl, fenchlorazole O ethyl, fenclorim, MG-191 (2-dichloromethyl-2-methyl-1,3-dioxane), cyometrinil, flurazole, fluxofenim, isoxadifen, isoxadifenethyl, mecoprop, MCPA, daimuron, 2,4-D, MON 4660 (code number), oxabetrinil, cyprosulfamide, lower alkyl-substituted benzoic acid, TI-35 (code number) and N-(2-methoxybenzoyl)-4-[(methylaminocarbonyl)amino]benzenesulfonamide (chemical name, CAS registration No.: 129531-12-0)

The pest control agent of the present invention constituted as above exhibits an excellent control effect to pest of Orthoptera, Thysanoptera, Hemiptera, Coleoptera, Diptera, Lepidoptera, Hymenoptera, Collembola, Thysanura, Blattodea, Isoptera, Psocoptera, Mallophaga, Anoplura, plant-feeding mites, plant parasitic nematodes, plant parasitic mollusk pests, other crop pests, nuisance pests, sanitary insects, parasites, etc. As examples of such pests, the following organism species can be mentioned.

As the Orthopteran pest, there can be mentioned, for example,

Tettigoniidae: Ruspolia lineosa, etc.,

Gryllidae: Teleogryllus emma, etc.,

Gryllotalpidae: Gryllotalpa orientalis,

Acrididae: Oxya hyla intricate, Locusta migratoria, Melanoplus sanguinipes, etc.,

Pyrgomorphidae: Atractomorpha lata,

Eneopteridae: Euscrytus japonicus,

Tridactylidae: Xya japonica, etc.

As the Thysanopteran pests, there can be mentioned, for example,

Thripidae: Frankliniella intonsa, Frankliniella occidentalis, Scirtothrips dorsalis, Thrips palmi, Thrips tabaci, etc.,

Phlaeothripidaes: Ponticulothrips diospyrosi, Haplothrips aculeatus, etc.

As the Hemipteran pests, there can be mentioned, for example,

Cicadidae: Mogannia minuta, etc.,

Aphrophoridae: Aphorphora intermedia, etc.,

Membracidae: Machaerotypus sibiricus, etc.,

Cicadellidae: Arboridia apicalis, Empoasca onukii, Nephotettix cincticeps, Recilia dorsalis, etc.,

Cixiidae: Pentastiridius apicalis, etc.,

Delphacidae: Laodelphax striatella, Nilaparvata lugens, Sogatella furcifera, etc.,

Meenoplidae: Nisia nervosa, etc.,

Derbidae: Kamendaka saccharivora, etc.,

Cixidia okunii: Achilus flammeus, etc.,

Ricaniidae: Orosanga japonicus, etc.,

Flatidae: Mimophantia maritima, etc.,

Psyllidae: Cacopsylla pyrisuga, etc.,

Calophyidae: Calophya mangiferae, etc.,

Phylloxeridae: Daktulosphaira vitifoliae, etc.,

Adelgidae: Adelges laricis, Adelges tsugae, etc.,

Aphydidae: Acyrthosiphon pisum, Aphis gossypii, Aphis spiraecola, Lipaphis erysimi, Myzus persicae, Schizaphis graminum, Rhopalosiphum padi, etc.,

Aleyrodidae: Aleurocanthus spiniferus, Bemisia tabaci, Bemisia argentifolii, Trialeurodes vaporariorum, etc.,

Margarodidae: Drosicha corpulenta, Icerya purchasi, etc.,

Pseudococcidae: Dysmicoccus brevipes, Planococcus citri, Pseudococcus comstocki, etc.,

Coccidae: Ceroplastes ceriferus, etc.,

Aclerdidae: Aclerda takahasii, etc.,

Diaspididae: Aonidella aurantii, Diaspidiotus perniciosus, Unaspis yanonensis, etc.,

Miridae: Lygus hesperus, Trigonotylus caelestialium, etc.,

Tingidae: Stephanitis pyrioides, Stephanitis nashi, etc.,

Pentatomidae: Eysarcoris aeneus, Lagynotomus elongatus, Nezara viridula, Plautia crossota, etc.,

Plataspidae: Megacopta cribaria, etc.,

Lygaeidae: Cavelerius saccharivorus, etc.,

Malcidae: Malcus japonicus, etc.,

Pyrrhocoridae: Dysdercus cingulatus, etc.,

Alydidae: Leptocorisa acuta, Leptocorisa chinensis, etc.,

Coreidae: Anacanthocoris striicornis, etc.,

Rhopalidae: Rhopalus maculatus, etc.,

Cimicidae: Cimex lectularius, etc.

As the Coleoptera pests, there can be mentioned, for example,

Scarabaeidae: Anomala cuprea, Anomala rufocuprea, Popillia japonica, Oryctes rhinoceros, etc.,

Elateridae: Agriotes ogurae fuscicollis, Melanotus okinawensis, Melanotos fortnumi fortnumi, etc.,

Dermestidae: Anthrenus verbasci, etc.,

Bostrychidae: Heterobostrychus hamatipennis, etc.,

Anobiidae: Stegobium paniceum, etc.,

Ptinidae: Pitinus clavipes, etc.,

Trogossitidae: Tenebroides mauritanicus, etc.,

Cleridae: Necrobia rufipes,

Nitidulidae: Carpophilus hemipterus, etc.,

Silvanidae: Ahasverus advena, etc.,

Laemophloeidae: Cryptolestes ferrugineus, etc.,

Coccinellidae: Epilachna varivestis, Henosepilachna vigintioctopunctata, etc.,

Tenebrionidae: Tenebrio molitor, Tribolium castaneum, etc.,

Meloidae: Epicauta gorhami, etc.,

Cerambycidae: Anoplophora glabripennis, Xylotrechus pyrrhoderus, Monochamus alternatus endai, etc.,

Bruchidae: Callosobruchus chinensis, etc.,

Chrysomelidae: Leptinotarsa decemlineata, Diabrotica virgifera, Phaedon brassicae, Phyllotreta striolata, etc.,

Brentidae: Cylas formicarius, etc.,

Curculionidae: Hypera postica, Listroderes costirostris, Euscepes postfasciatus, etc.,

Erirhinidae: Echinocnemus bipunctatus, Lissorhoptrus oryzophilus, etc.,

Dryophthoridae: Sitophilus zeamais, Sphenophrus vestitus, etc.,

Scolytidae: Tomicus piniperda, etc.,

Platypodidae: Crossotarsus niponicus, etc.,

Lyctidae: Lyctus brunneus, etc.

As the Diptera pests, there can be mentioned, for example,

Tipulidae: Tipila aino, etc.,

Bibionidae: Plecia nearctica, etc.,

Mycetophidae: Exechia shiitakevora, etc.,

Sciaridae: Pnyxia scabiei, etc.,

Cecidomyiidae: Asphondylia yushimai, Mayetiola destructor, etc.,

Culicidae: Aedes aegypti, Culex pipiens pallens, etc.,

Simuliidae: Simulim takahasii, etc.,

Chironomidae: Chironomus oryzae, etc.,

Tabanidae: Chrysops suavis, Tabanus trigonus, etc.,

Syrphidae: Eumerus strigatus, etc.,

Tephritidae: Bactrocera dorsalis, Euphranta japonia, Ceratitis capitata, etc.,

Agromyzidae: Liriomyza trifolii, Chromatomyia horticola, etc.,

Chloropidae: Meromyza nigriventris, etc.,

Drosophilidae: Drosophila suzukii, Drosophila melanogaster, etc.,

Ephydridae: Hydrellia griseola, etc.,

Hippoboscidae: Hippobosca equina, etc.,

Scatophagidae: Parallelpmma sasakawae, etc.,

Anthomyiidae: Delia antiqua, Delia platura, etc.,

Fanniidae: Fannia canicularis, etc.,

Muscidae: Musca domestica, Stomoxys calcitrans, etc.,

Sarcophagidae: Sarcophaga peregrina, etc.,

Gasterophilidae: Gasterophilus intestinalis, etc.,

Hypodermatidae: Hypoderma lineatum, etc.,

Oestridae: Oestrus ovis, etc.

As the Lepidoptera pests, there can be mentioned, for example,

Hepialidae: Endoclita excrescens, etc.,

Heliozelidae: Antispila ampelopsia, etc.,

Cossidae: Zeuzera multistrigata leuconota, etc.,

Tortricidae: Archips fuscocupreanus, Adoxophyes orana fasciata, Grapholita molesta, Homona magnanima, Leguminivora glycinivorella, Cydia pomonella, etc.,

Cochylidae: Eupoecilia ambiguella, etc.,

Psychidae: Bambalina sp., Eumeta minuscula, etc.,

Tineidae: Nemapogon granella, Tinea translucens, etc.,

Bucculatricidae: Bucculatrix pyrivorella, etc.,

Lyonetiidae: Lyonetia clerkella, etc.,

Gracilariidae: Caloptilia theivora, Phyllonorycter ringoniella, etc.,

Phyllocnistidae: Phyllocnistis citrella, etc.,

Acrolepiidae: Acrolepiopsis sapporensis, etc.,

Yponomeutidae: Plutella xylostella, Yponomeuta orientalis, etc.,

Argyresthidae: Argyresthia conjugella, etc.,

Sesidae: Nokona regalis, etc.,

Gelechiidae: Phthorimaea operculella, Sitotroga cerealella, Pectinophora gossypiella, etc.,

Carposinidae: Carposina sasakii, etc.,

Zygaenidae: Illiberis pruni, etc.,

Limacodidae: Monema flavescens, etc.,

Crambidae: Ancylolomia japonica, Chilo suppressalis, Cnaphalocrosis medinalis, Ostrinia furnacalis, Ostrinia nubilalis, etc.,

Pyralidae: Cadra cautella, Galleria mellonella, etc.,

Pterophoridae: Nippoptilia vitis, etc.,

Papilionidae: Papilio xuthus, etc.,

Pieridae: Pieris rapae crucivora, etc.,

Hesperiidae: Parnara guttata guttata, etc.,

Geometridae: Ascotis selenaria, etc.,

Lasiocampidae: Dendrolimus spectabilis, Malacosomaneustrium testaceum, etc.,

Sphingidae: Agrius convolvuli, etc.,

Lymantriidae: Arna pseudoconspersa, Lymantria dispar, etc.,

Arctiidae: Hyphantria cunea, etc.,

Noctuidae: Agrotis ipsilon, Autographa nigrisigna, Helicoverpa armigera, Helicoverpa zea, Heliothis virescens, Spodoptera exigua, Spodoptera litura, etc.

As the Hymenoptera pests, there can be mentioned, for example,

Argidae: Arge pagana, etc.,

Tenthredinidae: Apethymus kuri, Athalia rosae ruficornis, etc.,

Cynipidae: Dryocosmus kuriphilus, etc.,

Vespidae: Vespa simillima xanthoptera, etc.,

Formicidae: Solenopsis invicta, etc.,

Megachilidae: Megachile nipponica, etc.

As the Oder Collembola pests, there can be mentioned, for example,

Sminthuridae: Bourletiella hortensis, etc.

As the order Thysanura pests, there can be mentioned, for example,

Lepismatidae: Lepisma saccharina, Ctenolepisma villosa, etc.

As the Blattodea pests, there can be mentioned, for example,

Blattidae: Periplaneta americana,

Blattellidae: Blattella germanica, etc.

As the Order Isoptera pests, there can be mentioned, for example,

Kalotermitidae: Incisitermes minor, etc.,

Rhinotermitidae: Coptotermes formosanus, etc.,

Termitidae: Odontotermes formosanus, etc.

As the order Psocoptera pests, there can be mentioned, for example,

Trogiidae: Trogium pulsatorium, etc.,

Liposcelididae: Liposcelis corrodens, etc.

As the order Mallohaga pests, there can be mentioned, for example,

Menoponidae: Lipeurus caponis, etc.,

Trichodectidae: Damalinia bovis, etc.

As the order Anoplura pests, there can be mentioned, for example,

Haematopinidae: Haematopinus suis, etc.,

Pediculine: Pediculus humanus, etc.,

Linognathidae: Linognathus setosus, etc.,

Pthiridae: Phthrius pubis, etc.

As the plant-feeding mites, there can be mentioned, for example,

Eupodidae: Penthaleus major, etc.,

Tarsonemidae: Phytonemus pallidus, Polyphagotarsonemus latus, etc.,

Pyemotidae: Siteroptes sp., etc.,

Tenuipalpidae: Brevipalpus lewisi, etc.,

Tuckerellidae: Tuckerella pavoniformis, etc.,

Tetranychidae: Eotetranychus boreus, Panonychus citri, Panonychus ulmi, Tetranychus urticae, Tetranychus kanzawai, etc.,

Nalepellidae: Trisetacus pini, etc.,

Eriophyidae: Aculops pelekassi, Epitrimerus pyri, Phyllocoptruta oleivola, etc.,

Diptilomiopidae: Diptacus crenatae, etc.,

Acaridae: Aleuroglyphus ovatus, Tyrophagus putrescentiae, Rhizoglyphus robini, etc.

As the plant-parasitic nematodes, there can be mentioned, for example,

Longidoridae: Xiphinema index, etc.,

Trichodoridae: Paratrichodorus minor, etc.,

Rhabditidae: Rhabditella sp., etc.,

Tylenchidae: Aglenchus sp., etc.,

Tylodoridae: Cephalenchus sp., etc.,

Anguinidae: Nothotylenchus acris, Ditylenchus destructor, etc.,

Hoplolaimidae: Rotylenchulus reniformis, Helicotylenchus dihystera, etc.,

Paratylenchidae: Paratylenchus curvitatus, etc.,

Meloidogynidae: Meloidogyne incognita, Meloidogyne hapla, etc.,

Heteroderidae: Globodera rostochiensis, Heterodera glycines, etc.,

Telotylenchidae: Tylenchorhynchus claytoni etc.,

Psilenchidae: Psilenchus sp., etc.,

Criconematidae: Criconemoides sp., etc.,

Tylenchulidae: Tylenchulus semipenetrans, etc.,

Spaeronematidae: Sphaeronema camelliae, etc.,

Pratylenchidae: Radopholus citrophilus, Radopholus similis, Nacobbus aberrans, Pratylenchus penetrans, Pratylenchus coffeae, etc.,

Iotonchiidae: Iotonchium ungulatum, etc.,

Aphelenchidae: Aphelenchus avenae, etc.,

Aphelenchoididae: Aphelenchoides besseyi, Aphelenchoides fragariae, etc.,

Palasitaphelenchidae: Bursaphelenchus xylophilus, etc.

As the plant-parasitic mollusk pests, there can be mentioned, for example,

Pilidae: Pomacea canaliculata, etc.,

Veronicellidae: Leavicaulis alte, etc.,

Achatinidae: Achatina fulica, etc.,

Philomycidae: Meghimatium bilineatum, etc.,

Succineidae: Succinea lauta, etc.,

Didcidae: Discus pauper, etc.,

Zonitidae: Zonitoides yessoensis, etc.,

Limacidae: Limacus flavus, Deroceras reticulatum, etc.,

Helicarionidae: Parakaliella harimensis, etc.,

Bradybaenidae: Acusta despecta sieboldiana, Bradybaena similaris, etc.

As other pests such as injurious animals, uncomfortable animals, sanitary insects, livestock insects, parasites and the like, there can be mentioned, for example,

Acari Macronysshidae: Ornithonyssus sylvialum, etc.,

Varroidae: Varroa jacobsoni, etc.,

Dermanyssidae: Dermanyssus gallinae, etc.,

Macronyssidae: Ornithonyssus sylvialum, etc.,

Ixodidae: Boophilus microplus, Rhipicephalus sanguineus, Haemaphysalis longicornis, etc.,

Sacroptidae: Sarcoptes scabiei, etc.,

Isopoda Armadillididae: Armadillidium vulgare, etc.,

Decapoda Astacidae: Procambarus clarkii, etc.,

Porcellionidae: Armadillidium vulgare, etc.,

Chilopoda pests: Scutigeromorpha Sutigeridae, Thereuonema tuberculata, Scolopendromorpha Scolopendra subpinipes, etc.

Diplopoda pests: Polydesmida Paradoxosomatidae Oxidus gracillis, etc.

Araneae Latrodectus hasseltii: Theridiiadae hasseltii, etc.,

Clubionidae: Chiracanthium japonicum, etc.,

Order Scorpionida: Androctonus crassicauda, etc.,

Parasitic roundworm: Ascaris lumbricoides, Syphacia sp., Wucherebia bancrofti, etc.,

Parasitic flatworm: Distomum sp., Paragonimus westermanii, Metagonimus yokokawai, Schistosoma japonicum, Taenia solium, Taeniarhynchus saginatus, Echinococcus sp., Diphyllobothrium latum, etc.

The present pest control agent exhibits control effect also to the above-mentioned pests, etc., which already have resistances to existing pest control agents. Furthermore, the present control agent can be applied to plants which already have resistances to insects, diseases, herbicides, etc., owing to genetic modification, artificial mating, etc.

Next, there are described the production methods, formulation methods and applications of the present compound, in detail by way of Examples. However, the present invention is in no way restricted by these Examples.

There are also described the production methods of the intermediates for production of the present compound.

EXAMPLES Example 1 Production of 2-fluoro-4-methyl-5-(2,2,2-trifluoroethylthio)phenol (Present Compound No. C-0001)

To 300 ml of toluene were added 32.0 g (119 mmol) of 2-fluoro-4-methyl-5-(2,2,2-trifluoroethylthio)phenyl boronic acid produced by the method described in PCT International Publication No. WO 2007/034755 and 15.4 g (131 mmol) of N-methylmorpholine-N-oxide, followed by refluxing for 1 hour under heating. The reaction mixture was allowed to cool to room temperature. The solvent was distilled off under reduced pressure. The residue was subjected to extraction with ethyl acetate. The organic phase obtained was washed with water and then dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (developing solvent: a mixed solvent of n-hexane:ethyl acetate=4:1), to obtain 25.5 g (yield: 89%) of an intended product.

¹H-NMR (300 MHz, CDCl₃/TMS δ (ppm))

2.38 (3H, s), 3.32 (2H, q), 5.28 (1H, brs),

6.95 (1H, d), 7.22 (1H, d)

Example 2 Production of 4-methyl-3-(2,2,2-trifluoroethylthio)phenol (Present Compound No. C-0005)

49.7 g (225 mmol) of 4-methyl-3-(2,2,2-trifluoroethylthio)aniline was suspended in 500 ml of a 15% aqueous sulfuric acid solution. Thereinto was dropwise added an aqueous solution obtained by dissolving 18.6 g (270 mmol) of sodium nitrite in 100 ml of water, at 0 to 5° C. with ice-cooling. After the completion of the dropwise addition, the mixture was stirred for 1 hour with the temperature being kept. The reaction mixture was gradually dropped at 120° C. into a solution obtained by dissolving 71.8 g (450 mmol) of anhydrous copper sulfate in 400 ml of 60% sulfuric acid. The mixture was allowed to cool to room temperature and subjected to extraction with ethyl acetate. The organic phase obtained was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The crude product obtained was purified by column chromatography (developing solvent: a mixed solvent of n-hexane:ethyl acetate=10:1), to obtain 19 g (yield: 38%) of an intended product.

¹H-NMR (400 MHz, CDCl₃/TMS δ (ppm))

2.36 (3H, s), 3.38 (2H, q), 5.61 (1H, brs),

6.69 (1H, dd), 6.93 (1H, s), 7.03 (1H, d)

Example 3 Production of 5,5-dimethylhexyl-[2-fluoro-4-methyl-5-(2,2,2-trifluoroethylthio)phenyl] ether (Present Compound No. A-0085)

To 70 ml of tetrahydrofuran were added 1.6 g (6.7 mmol) of 2-fluoro-4-methyl-3-(2,2,2-trifluoroethylthio)phenol, 1.7 g (13 mmol) of 5,5-dimethylhexanol, 2.0 g (9.9 mmol) of diisopropyl azodicarboxylate and 2.6 g (9.9 mmol) of triphenylphosphine. A reaction was carried out at room temperature for 16 hours. After confirmation of the completion of the reaction, the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (developing solvent: a mixed solvent of n-hexane:ethyl acetate=4:1), to obtain 2.3 g (yield: 97%) of an intended product.

Incidentally, the production method of 5,5-dimethylhexanol is described in, for example, J. Am. Chem. Soc., 119 (29), 6909 (1997).

¹H-NMR (300 MHz, CDCl₃/TMS δ (ppm))

0.88 (9H, s), 1.19-1.27 (2H, m), 1.36-1.48 (2H, m),

1.77 (2H, quint), 2.41 (3H, s), 3.29 (2H, q),

4.01 (2H, t), 6.95 (1H, d), 7.15 (1H, d)

Example 4 Production of 5,5-dimethylhexyl-[2-fluoro-4-methyl-5-(2,2,2-trifluoroethylsulfinyl)phenyl] ether (Present Compound No. A-0086)

In 70 ml of chloroform was dissolved 2.3 g (6.5 mmol) of 5,5-dimethylhexyl-{2-fluoro-4-methyl-5-(2,2,2-trifluoroethylthio)phenyl ether. Thereto was added, in portions in about 10 minutes, 1.5 g (6.5 mmol) of 3-chloroperbenzoic acid (purity: about 75%) at room temperature. A reaction was carried out for 1 hour. After confirmation of the completion of the reaction, the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (developing solvent: a mixed solvent of n-hexane:ethyl acetate:triethylamine=5:1:0.01), to obtain 2.2 g (yield: 92%) of an intended product.

¹H-NMR (300 MHz, CDCl₃/TMS δ (ppm))

0.89 (9H, s), 1.19-1.27 (2H, m), 1.37-1.49 (2H, m),

1.81 (2H, quint), 2.31 (3H, s), 3.30-3.48 (2H, m),

4.10 (2H, t), 6.98 (1H, d), 7.55 (1H, d)

Example 5 Production of 5-trifluoromethylthiopentyl-[4-methyl-3-(2,2,2-trifluoroethylthio)phenyl] ether (Present Compound No. A-0438)

To 100 ml of tetrahydrofuran were added 1.5 g (4.3 mmol) of 5-thiocyanatopentyl-{4-methyl-3-(2,2,2-trifluroethylthio)phenyl} ether and 1.8 g (13 mmol) of trifluoromethyltrimetylsilane. Thereto was added, at 0° C., 5 ml (5.0 mmol) of a tetra-n-butylammonium fluoridetetrahydrofuran (1 mol/liter) solution. A reaction was carried out for 1 hour. After confirmation of the completion of the reaction, the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (developing solvent: a mixed solvent of n-hexane:ethyl acetate=10:1), to obtain 1.3 g (yield: 77%) of an intended product.

¹H-NMR (300 MHz, CDCl₃/TMS δ (ppm))

1.56-1.64 (2H, m), 1.73-1.85 (4H, m), 2.38 (3H, s),

2.91 (2H, t), 3.40 (2H, q), 3.94 (2H, t), 6.75 (1H, dd), 7.00 (1H, d), 7.11 (1H, d)

Example 6 Production of 5-chloropentyl-[4-methyl-3-(2,2,2-trifluoroethylthio)phenyl] ether (Present Compound No. A-0279)

To 100 ml of acetonitrile were added 2.5 g (11 mmol) of 4-methyl-3-(2,2,2-trifluoroethylthio)phenol, 2.5 g (13 mmol) of 1-bromo-5-chloropentane, 1.9 g (14 mmol) of potassium carbonate and 0.35 g (1.1 mmol) of tetra-n-butylammonium bromide. The mixture was refluxed for 5 hours under heating and then allowed to cool to room temperature. The solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (developing solvent: a mixed solvent of n-hexane:ethyl acetate=10:1), to obtain 2.9 g (yield: 79%) of an intended product.

¹H-NMR (300 MHz, CDCl₃/TMS δ (ppm))

1.56-1.66 (2H, m), 1.74-1.93 (4H, m), 2.38 (3H, s),

3.36 (2H, q), 3.56 (2H, t), 3.94 (2H, t), 6.74 (1H, d), 7.00 (1H, s), 7.09 (1H, d)

Example 7 Production of 5-thiocyanatopentyl-[4-methyl-3-(2,2,2-trifluoroethylthio)phenyl] ether (Present Compound No. A-0672)

To 100 ml of ethanol were added 2.0 g (6.1 mmol) of 5-chloropentyl-{4-methyl-3-(2,2,2-trifluoroethylthio)phenyl} ether, 4.0 g (41 mmol) of potassium thiocyanate and 0.10 g (0.61 mmol) of potassium iodide. The mixture was refluxed for 10 hours under heating and then allowed to cool to room temperature. The solvent was distilled off under reduced pressure. To the residue was added ethyl acetate to conduct extraction. The organic phase obtained was washed with water and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (developing solvent: a mixed solvent of n-hexane:ethyl acetate=10:1), to obtain 1.8 g (yield: 84%) of an intended product.

¹H-NMR (300 MHz, CDCl₃/TMS δ (ppm))

1.53-1.68 (2H, m), 1.76-1.87 (4H, m), 2.38 (3H, s),

3.00 (2H, t), 3.39 (2H, q), 3.97 (2H, t), 6.74 (1H, d), 7.00 (1H, s), 7.13 (1H, d)

Example 8 Production of 5-trifluoromethylthiopentyl-[4-methyl-3-(2,2,2-trifluoroethylsulfinyl)phenyl] ether (Present Compound No. A-0439)

In 100 ml of chloroform was dissolved 0.98 g (2.5 mmol) of 5-trifluoromethylthiopentyl-{4-methyl-5-(2,2,2-trifluoroethylthio)phenyl} ether. Thereto was added, in portions in about 10 minutes, 0.58 g (2.5 mmol) of 3-chloroperbenzoic acid (purity: about 75%) at room temperature. A reaction was carried out for 1 hour. After confirmation of the completion of the reaction, the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (developing solvent: a mixed solvent of n-hexane:ethyl acetate:triethylamine=5:1:0.01), to obtain 0.78 g (yield: 77%) of an intended product.

¹H-NMR (300 MHz, CDCl₃/TMS δ (ppm))

1.57-1.64 (2H, m), 1.73-1.88 (4H, m), 2.31 (3H, s),

2.92 (2H, t), 2.32-3.45 (2H, m), 4.05 (2H, t),

6.97 (1H, dd), 7.15 (1H, d), 7.48 (1H, d)

Example 9 Production of 4-chloro-2-fluoro-5-(2,2,2-trifluoroethylthio)phenol (Present Compound No. C-0003)

To 200 ml of toluene were added 33 g (114 mmol) of 4-chloro-2-fluoro-5-(2,2,2-trifluoroethylthio)phenyl boronic acid and 16 g (137 mmol) of N-methylmorpholine-N-oxide. The mixture was refluxed for 1 hour under heating. After confirmation of the completion of the reaction, the mixture was allowed to cool to room temperature. Then the solvent was distilled off under reduced pressure, and the residue was subjected to extraction with ethyl acetate. The organic phase obtained was washed with water and dried over anhydrous magnesium sulfate and the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography to obtain 24.5 g (yield: 82%) of an intended product.

¹H-NMR (300 MHz, CDCl₃/TMS δ (ppm))

3.43 (2H, q), 5.31 (1H, d), 7.16 (1H, d), 7.31 (1H, d)

Example 10 Production of 5-bromopentyl-[4-chloro-2-fluoro-5-(2,2,2-trifluoroethylthio)phenyl] ether (Present Compound No. A-0273)

To 60 ml of acetonitrile were added 3.0 g (11.5 mmol) of 4-chloro-2-fluoro-5-(2,2,2-trifluoroethylthio)phenol, 13.2 g (57.4 mmol) of 1,5-dibromopentane, 2.1 g (15.0 mmol) of potassium carbonate and 0.37 g (1.15 mmol) of tetra-n-butylammonium bromide. The mixture was refluxed for 1.5 hour under heating. The mixture was allowed to cool to room temperature, and insoluble matters were removed by filtration. Then the filtrate was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (developing solvent: a mixed solvent of n-hexane:ethyl acetate=20:1), to obtain 4.2 g (yield: 89%) of an intended product.

¹H-NMR (400 MHz, CDCl₃/TMS δ (ppm))

1.59-1.69 (2H, m), 1.82-1.99 (4H, m), 3.36-3.47 (4H, m), 4.03 (2H, t), 7.20 (1H, d), 7.23 (1H, d)

Example 11 Production of 5-thiocyanatopentyl-[4-chloro-2-fluoro-5-(2,2,2-trifluoroethylthio)phenyl] ether (Present Compound No. A-0670)

To 60 ml of ethanol were added 4.2 g (10.3 mmol) of 5-bromopentyl-[4-chloro-2-fluoro-5-(2,2,2-trifluoroethylthio)phenyl] ether and 5.0 g (51.5 mmol) of potassium thiocyanate. The mixture was refluxed for 4 hours under heating. The mixture was allowed to cool to room temperature, and the solvent was distilled off under reduced pressure. Then extraction was conducted by adding water and ethyl acetate. The organic phase obtained was dried over anhydrous magnesium sulfate and the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (developing solvent: a mixed solvent of n-hexane:ethyl acetate=10:1), to obtain 3.9 g (yield: 98%) of an intended product.

¹H-NMR (400 MHz, CDCl₃/TMS δ (ppm))

1.59-1.69 (2H, m), 1.82-1.99 (4H, m), 2.99 (2H, t)

3.42 (2H, q), 4.04 (2H, t), 7.20 (1H, d), 7.23 (1H, d)

Example 12 Production of 5-trifluoromethylthiopentyl-[4-chloro-2-fluoro-5-(2,2,2-trifluoroethylthio)phenyl] ether (Present Compound No. A-0433)

To 60 ml of tetrahydrofuran were added 3.9 g (10.1 mmol) of 5-thiocyanatopentyl-[4-chloro-2-fluoro-5-(2,2,2-trifluoroethylthio)phenyl] ether and 4.5 g (31.6 mmol) of trifluoromethyltrimethylsilane. Thereto was added 1.0 ml (1.04 mmol) of tetrahydrofuran solution (1 mol/liter) of tetra-n-butylammonium fluoride at 0° C., and reaction was carried out. The mixture was stirred overnight at room temperature. Then, the solvent was distilled off under reduced pressure, and the residue was purified by silica gel column chromatography (developing solvent: a mixed solvent of n-hexane:ethyl acetate=20:1), to obtain 2.60 g (yield: 60%) of an intended product.

¹H-NMR (400 MHz, CDCl₃/TMS δ (ppm))

1.58-1.66 (2H, m), 1.73-1.89 (4H, m), 2.92 (2H, t),

3.41 (2H, q), 4.03 (2H, t), 7.21 (1H, d), 7.23 (1H, d)

Example 13 Production of 5-trifluoromethylthiopentyl-[4-chloro-2-fluoro-5-(2,2,2-trifluoroethylsulfinyl)phenyl] ether (Present Compound No. A-0434)

In 50 ml of chloroform was dissolved 2.60 g (6.03 mmol) of 5-trifluoromethylthiopentyl-[4-chloro-2-fluoro-5-(2,2,2-trifluoroethylthio)phenyl] ether. Thereto was added 1.39 g (6.04 mmol) of 3-chloroperbenzoic acid (purity: about 75%) at 0° C., and the mixture was stirred overnight at room temperature. Then, the solvent was distilled off under reduced pressure, 1 ml of triethylamine was added to the residue, and the residue was purified by silica gel column chromatography (developing solvent: a mixed solvent of n-hexane:ethyl acetate=5:1), to obtain 2.06 g (yield: 76%) of an intended product.

¹H-NMR (400 MHz, CDCl₃/TMS δ (ppm))

1.57-1.66 (2H, m), 1.74-1.93 (4H, m), 2.92 (2H, t),

3.30-3.43 (1H, m), 3.66-3.78 (1H, m), 4.13 (2H, t),

7.21 (1H, d), 7.54 (1H, d)

Example 14 Production of 2,4-dichloro-5-(2,2,2-trifluoroethylthio)phenol (Present Compound No. C-0014)

To 150 ml of toluene was added 29.0 g (50% aqueous solution, 124 mmol) of N-methylmorpholine-N-oxide, and dehydration was conducted by heating under reflux for 1 hour. To the reaction mixture was dropwise added 31.5 g (103 mmol) of 2,4-dichloro-5-(2,2,2-trifluoroethylthio)phenylboronic acid dissolved in ethyl acetate, and the mixture was refluxed for 3 hours under heating. Then, the mixture was allowed to cool to room temperature, and 10% aqueous hydrochloric acid was added, followed by extraction with ethyl acetate. The organic phase obtained was washed with saturated sodium chloride solution, dried over anhydrous magnesium sulfate and the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (developing solvent: a mixed solvent of n-hexane:ethyl acetate=10:1), to obtain 27.2 g (yield: 95%) of an intended product.

¹H-NMR (300 MHz, CDCl₃/TMS δ (ppm))

3.48 (2H, q), 5.70 (1H, s), 7.20 (1H, s), 7.41 (1H, s)

Example 15 Production of 6-bromohexyl-[2,4-dichloro-5-(2,2,2-trifluoroethylthio)phenyl] ether (Present Compound No. A-0283)

To 30 ml of acetonitrile were added 1.0 g (3.61 mmol) of 2,4-dichloro-5-(2,2,2-trifluoroethylthio)phenol, 3.5 g (14.4 mmol) of 1,6-dibromohexane, 0.65 g (15.0 mmol) of potassium carbonate and 0.12 g (0.37 mmol) of tetra-n-butylammonium bromide. The mixture was refluxed for 3 hours under heating. The mixture was allowed to stand at room temperature, and insoluble matters were removed by filtration. Then the filtrate was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (developing solvent: a mixed solvent of n-hexane:ethyl acetate=20:1), to obtain 1.51 g (yield: 95%) of an intended product.

¹H-NMR (400 MHz, CDCl₃/TMS δ (ppm))

1.50-1.60 (4H, m), 1.81-1.93 (4H, m),

3.39-3.49 (4H, m), 4.02 (2H, t), 7.13 (1H, s),

7.45 (1H, s)

Example 16 Production of 6-thiocyanatohexyl-[2,4-dichloro-5-(2,2,2-trifluoroethylthio)phenyl] ether (Present Compound No. A-0678)

In 30 ml of ethanol were added 1.51 g (3.43 mmol) of 6-bromohexyl-[2,4-dichloro-5-(2,2,2-trifluoroethylthio)phenyl] ether and 1.67 g (17.2 mmol) of potassium thiocyanate. The mixture was refluxed for 3 hours under heating. The mixture was allowed to cool to room temperature, and the solvent was distilled off under reduced pressure. Then extraction was conducted by adding ethyl acetate and water. The organic phase obtained was dried over anhydrous magnesium sulfate and the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (developing solvent: a mixed solvent of n-hexane:ethyl acetate=10:1), to obtain 1.04 g (yield: 73%) of an intended product.

¹H-NMR (400 MHz, CDCl₃/TMS δ (ppm))

1.50-1.62 (4H, m), 1.83-1.92 (4H, m), 2.96 (2H, t),

3.45 (2H, q), 4.03 (2H, t), 7.13 (1H, s), 7.46 (1H, s)

Example 17 Production of 6-trifluoromethylthiohexyl-[2,4-dichloro-5-(2,2,2-trifluoroethylthio)phenyl] ether (Present Compound No. A-0478)

To 30 ml of tetrahydrofuran were added 1.04 g (2.49 mmol) of 6-thiocyanatohexyl-[2,4-dichloro-5-(2,2,2-trifluoroethylthio)phenyl] ether and 1.06 g (7.45 mmol) of trifluoromethyltrimethylsilane. Thereto was added 0.25 ml (concentration: 1 mol/liter, 0.25 mmol) of tetrahydrofuran solution of tetra-n-butylammonium fluoride at 0° C., and reaction mixture was stirred for 2 hours at room temperature. Then, the solvent was distilled off under reduced pressure, and the residue was purified by silica gel column chromatography (developing solvent: a mixed solvent of n-hexane:ethyl acetate=20:1), to obtain 0.73 g (yield: 64%) of an intended product.

¹H-NMR (300 MHz, CDCl₃/TMS δ (ppm))

1.44-1.62 (4H, m), 1.67-1.90 (4H, m), 2.90 (2H, t),

3.44 (2H, q), 4.02 (2H, t), 7.13 (1H, s), 7.46 (1H, s)

Example 18 Production of 6-trifluoromethylthiohexyl-[2,4-dichloro-5-(2,2,2-trifluoroethylsulfinyl)phenyl] ether (Present Compound No. A-0479)

In 30 ml of chloroform was dissolved 0.53 g (1.15 mmol) of 6-trifluoromethylthiohexyl-[2,4-dichloro-5-(2,2,2-trifluoroethylthio)phenyl] ether. Thereto was added 0.26 g (1.13 mmol) of 3-chloroperbenzoic acid (purity: about 75%) at 0° C., and the mixture was stirred for 3 hours at room temperature. Then, the solvent was distilled off under reduced pressure, 0.5 ml of triethylamine was added to the residue, and the residue was purified by silica gel column chromatography (developing solvent: a mixed solvent of n-hexane:ethyl acetate=5:1), to obtain 0.41 g (yield: 75%) of an intended product.

¹H-NMR (300 MHz, CDCl₃/TMS δ (ppm))

1.48-1.64 (4H, m), 1.63-1.94 (4H, m), 2.90 (2H, t),

3.28-3.44 (1H, m), 3.68-3.81 (1H, m), 4.13 (2H, t)

7.47 (1H, s), 7.48 (1H, s)

Example 19 Production of 2,4-dichloro-5-(2,2,2-trifluoroethylsulfinyl)phenol (Present Compound No. C-0015)

In 80 ml of chloroform was dissolved 10.0 g (36.08 mmol) of 2,4-dichloro-5-(2,2,2-trifluoroethylthio)phenol. Thereto was added 9.80 g (39.75 mmol) of 3-chloroperbenzoic acid (purity: about 70%) under ice cooling, and the mixture was stirred for 30 minutes at room temperature. Then, saturated aqueous solution of sodium thiosulfate was added to the reaction mixture to decompose excess peroxide. Thereafter, the solvent was distilled off under reduced pressure, and extraction was conducted by adding ethyl acetate and water. The organic phase obtained was washed by aqueous potassium carbonate solution and saturated aqueous sodium chloride solution in this order, and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, to obtain 9.30 g (yield: 88%) of an intended product.

¹H-NMR (300 MHz, CDCl₃/TMS δ (ppm))

3.30-3.44 (1H, m), 3.66-3.80 (1H, m), 7.40 (1H, s),

7.61 (1H, s)

Example 20 Production of 2-(4-trifluoromethylphenyl)ethyl-[2,4-dichloro-5-(2,2,2-trifluoroethylsulfinyl)phenyl] ether (Present Compound No. A-0767)

In 30 ml of tetrahydrofuran were dissolved 0.5 g (1.71 mmol) of 2,4-dichloro-5-(2,2,2-trifluoroethylsulfinyl)phenol, 0.33 g (1.74 mmol) of 2-(4-trifluoromethylphenyl)ethanol and 0.49 g (1.87 mmol) of triphenylphosphine. Thereto was added 0.38 g (1.87 mmol) of diisopropyl azodicarboxylate at room temperature, and the reaction mixture was stirred for 16 hours. Then, the solvent was distilled off under reduced pressure, and the residue was purified by silica gel column chromatography (developing solvent: a mixed solvent of n-hexane:ethyl acetate=5:1), to obtain 0.41 g (yield: 52%) of an intended product.

¹H-NMR (300 MHz, CDCl₃/TMS δ (ppm))

3.21-3.40 (3H, m), 3.64-3.79 (1H, m), 4.31-4.36 (2H, m), 7.44-7.46 (4H, m), 7.58 (2H, d)

Example 21 Production of 2,4-dimethyl-5-(2,2,2-trifluoroethylthio)phenol (Present Compound No. C-0017)

To 200 ml of toluene were added 20.24 g (58.5 mmol) of [2,4-dimethyl-5-(2,2,2-trifluoroethylthio)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (a compound described in PCT International Publication No. WO 2012/176856 as Compound No. 55-47) and 8.22 g (70.16 mmol) of N-methylmorpholine-N-oxide. The mixture was refluxed for 2 hours under heating. The reaction mixture was allowed to cool to room temperature, washed and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure and the residue was purified by silica gel column chromatography (developing solvent: a mixed solvent of n-hexane:ethyl acetate=20:1), to obtain 10.54 g (yield: 76%) of an intended product.

¹H-NMR (300 MHz, CDCl₃/TMS δ (ppm))

2.20 (3H, s), 2.36 (3H, s), 3.32 (2H, q), 4.78 (1H, s), 6.93 (1H, s), 6.98 (1H, s)

Example 22 Production of 2,4-dimethyl-5-(2,2,2-trifluoroethylsulfinyl)phenol (Present Compound No. C-0018)

In 30 ml of chloroform was dissolved 2.60 g (11.0 mmol) of 2,4-dimethyl-5-(2,2,2-trifluoroethylthio)phenol. Thereto was added 3.25 g (13.18 mmol) of 3-chloroperbenzoic acid (purity: about 70%) under ice cooling, and the mixture was stirred for 30 minutes at room temperature. Then, saturated aqueous solution of sodium thiosulfate was added to the reaction mixture to decompose excess peroxide. Thereafter, the solvent was distilled off under reduced pressure, and phase separation was conducted by adding ethyl acetate and water. The organic phase obtained was washed by aqueous potassium carbonate solution and saturated aqueous sodium chloride solution, and dried over magnesium sulfate. The solvent was distilled off under reduced pressure, to obtain 2.13 g (yield: 77%) of an intended product.

¹H-NMR (300 MHz, CDCl₃/TMS δ (ppm))

2.25 (6H, s), 3.35-3.53 (2H, m), 6.98 (1H, s),

7.63 (1H, s), 7.69 (1H, s)

Example 23 Production of 2-(4′-trifluoromethoxyphenyl)ethyl-[2,4-dimethyl-5-(2,2,2-trifluoroethylsulfinyl)phenyl] ether (Present Compound No. A-0783)

In 30 ml of tetrahydrofuran were dissolved 0.3 g (1.19 mmol) of 2,4-dimethyl-5-(2,2,2-trifluoroethylsulfinyl)phenol, 0.29 g (1.41 mmol) of 2-(4′-trifluoromethoxyphenyl)ethanol and 0.41 g (1.56 mmol) of triphenylphosphine. Thereto was added 0.31 g (1.53 mmol) of diisopropyl azodicarboxylate at room temperature, and stirred for 16 hours. The solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (developing solvent: a mixed solvent of n-hexane:ethyl acetate=5:1), and the residue was washed with n-hexane, to obtain 0.21 g (yield: 40%) of an intended product.

¹H-NMR (300 MHz, CDCl₃/TMS δ (ppm))

2.18 (3H, s), 2.26 (3H, s), 3.13 (2H, t),

3.32-3.41 (2H, m), 4.24-4.25 (2H, m),

6.70 (1H, s), 7.16 (2H, d), 7.30-7.36 (3H, m)

Example 24 Production of 6-bromohexyl-[2,4-dimethyl-5-(2,2,2-trifluoroethylthio)phenyl] ether (Present Compound No. A-0284)

To 60 ml of acetonitrile were added 1.14 g (4.83 mmol) of 2,4-dimethyl-5-(2,2,2-trifluoroethylthio)phenol, 4.71 g (19.31 mmol) of 1,6-dibromohexane, 0.73 g (5.28 mmol) of potassium carbonate and catalytic amount of tetra-n-butylammonium bromide. The mixture was refluxed for 3 hours under heating. The mixture was allowed to cool to room temperature, and insoluble matters were removed by filtration. Then the solvent of filtrate was distilled off under reduced pressure, and the residue was purified by silica gel column chromatography (developing solvent: a mixed solvent of n-hexane:ethyl acetate=40:1-20:1), to obtain 1.87 g (yield: 97%) of an intended product.

¹H-NMR (300 MHz, CDCl₃/TMS δ (ppm))

1.53 (4H, m), 1.70-2.03 (4H, m), 2.17 (3H, s),

2.38 (3H, s), 3.26-3.43 (4H, m), 3.94 (2H, t),

6.96 (1H, s), 6.99 (1H, s)

Example 25 Production of 6-thiocyanatohexyl-[2,4-dimethyl-5-(2,2,2-trifluoroethylthio)phenyl] ether (Present Compound No. A-0679)

To 60 ml of ethanol were added 1.87 g (4.68 mmol) of 6-bromohexyl-[2,4-dimethyl-5-(2,2,2-trifluoroethylthio)phenyl] ether and 2.28 g (23.46 mmol) of potassium thiocyanate. The mixture was refluxed for 8 hours under heating. The mixture was allowed to cool to room temperature, and the solvent was distilled off under reduced pressure. Then extraction was conducted by adding ethyl acetate and water. The organic phase obtained was washed with water, and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (developing solvent: a mixed solvent of n-hexane:ethyl acetate=20:1), to obtain 1.37 g (yield: 77%) of an intended product.

¹H-NMR (300 MHz, CDCl₃/TMS δ (ppm))

1.53-1.54 (4H, m), 1.82-1.87 (4H, m), 2.17 (3H, s)

2.38 (3H, s), 2.96 (2H, t), 3.31 (2H, q), 3.94 (2H, t)

6.96 (1H, s), 6.70 (1H, s)

Example 26 Production of 6-trifluoromethylthiohexyl-[2,4-dimethyl-5-(2,2,2-trifluoroethylthio)phenyl] ether (Present Compound No. A-0480)

To 100 ml of tetrahydrofuran were added 1.37 g (3.63 mmol) of 6-thiocyanatohexyl-[2,4-dimethyl-5-(2,2,2-trifluoroethylthio)phenyl] ether and 1.29 g (9.07 mmol) of trifluoromethyltrimethylsilane. Thereto was added 0.4 ml (0.4 mmol) of tetrahydrofuran solution of tetra-n-butylammonium fluoride (1 mol/liter) at 0° C., and the mixture was stirred for 4 hours at 0° C. Then, the solvent was distilled off under reduced pressure, and the residue was purified by silica gel column chromatography (developing solvent: a mixed solvent of n-hexane:ethyl acetate=20:1), to obtain 1.36 g (yield: 89%) of an intended product.

¹H-NMR (300 MHz, CDCl₃/TMS δ (ppm))

1.49-1.53 (4H, m), 1.71-1.82 (4H, m), 2.17 (3H, s)

2.38 (3H, s), 2.90 (2H, t), 3.30 (2H, q), 3.94 (2H, t)

6.96 (1H, s), 6.70 (1H, s)

Example 27 Production of 6-trifluoromethylthiohexyl-[2,4-dimethyl-5-(2,2,2-trifluoroethylsulfinyl)phenyl]ether (Present Compound No. A-0481)

In 40 ml of chloroform was dissolved 1.36 g (3.23 mmol) of 6-trifluoromethylthiohexyl-[2,4-dimethyl-5-(2,2,2-trifluoroethylthio)phenyl]ether. Thereto was added 0.67 g (2.72 mmol) of 3-chloroperbenzoic acid (purity: about 70%) under ice cooling, and the mixture was stirred for 30 minutes at room temperature. Then, saturated aqueous solution of sodium thiosulfate was added to the reaction mixture to decompose excess peroxide. Thereafter, the solvent was distilled off under reduced pressure, and extraction was conducted by adding ethyl acetate and water. The organic phase obtained was washed by aqueous potassium carbonate solution and saturated aqueous sodium chloride solution in this order, and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and the residue was purified by silica gel column chromatography (developing solvent: a mixed solvent of n-hexane:ethyl acetate=5:1), to obtain 0.87 g (yield: 62%) of an intended product.

¹H-NMR (400 MHz, CDCl₃/TMS δ (ppm))

1.50-1.52 (4H, m), 1.72-1.85 (4H, m), 2.23 (3H, s),

2.28 (3H, s), 2.90 (2H, t), 3.28-3.47 (2H, m),

4.04 (2H, t), 7.01 (1H, s), 7.36 (1H, s)

Example 28 Production of 5-trifluoromethylthiopentyl-[4-chloro-2-fluoro-5-(2,2,2-trifluoroethylsulfinyl)phenyl]ether optical isomer

An optical active column (internal diameter: 20 mm, length: 250 mm), CHIRAL PAK AD (trade name) manufactured by Daicel Corporation, was equipped with high performance liquid chromatography equipment, and a mixed solvent (hexane:2-propanol=97:3) was perfused as mobile phase. Then, 150 mg of 5-trifluoromethylthiopentyl-[4-chloro-2-fluoro-5-(2,2,2-trifluoroethylsulfinyl)phenyl]ether (racemic mixture) dissolved in 2-propanol was injected, and analysis was conducted in a following conditions.

flow speed: 8.0 ml/minute temperature: room temperature detector: ultraviolet absorption detector (254 nm) As a result, there observed peak 1 (retention time: 17.8 minutes) and peak 2 (retention time: 30.2 minutes), and 70 mg of a compound of respective peaks (both optical purity was 100% e.e.) were isolated. Measurement of respective Reflective Index revealed that Specific Rotation of the component of peak 1 was [α]_(D) ²⁵=−120.28° (C=0.50/methanol) and Specific Rotation of the component of peak 2 was [α]_(D) ²⁵=+119.32° (C=0.50/methanol).

Accordingly, the component of the peak 1 is (−)-5-trifluoromethylthiopentyl-[4-chloro-2-fluoro-5-(2,2,2-trifluoroethylsulfinyl)phenyl]ether [(−)-enantiomer of the present compound No. A-0434], and the component of the peak 2 is (+)-5-trifluoromethylthiopentyl-[4-chloro-2-fluoro-5-(2,2,2-trifluoroethylsulfinyl)phenyl]ether [(+)-enantiomer of the present compound No. A-0434].

Reference Example 1 Production of p-acetotoluidine

100 g (933.3 mmol) of p-toluidine and 154.8 g (1,120 mmol) of potassium carbonate were dissolved in a mixed solvent of 1,000 ml of ethyl acetate and 500 ml of water. Thereinto was dropped 87.9 g (1,120 mmol) of acetyl chloride with ice-cooling, followed by stirring for 2 hours. Extraction with ethyl acetate was carried out. The organic phase obtained was dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure. The crude crystal obtained was washed with hexane to obtain 130 g (yield: 93%) of p-acetotoluidine.

¹H-NMR (400 MHz, CDCl₃/TMS δ (ppm))

2.16 (3H, s), 2.31 (3H, s), 7.11-7.16 (3H, m),

7.37 (2H, d)

Reference Example 2 Production of 3-chlorosulfonyl-4-methylacetoanilide

130 g (871 mmol) of p-acetotoluidine was gradually added to 405 g (3,477 mmol) of chlorosulfonic acid at room temperature, followed by stirring at 60° C. for 1 hour. The reaction mixture was allowed to stand at room temperature and then poured into ice water. Extraction with ethyl acetate was conducted. The organic phase obtained was dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure to obtain 162 g (yield: 75%) of 3-chlorosulfonyl-4-methylacetoanilide.

¹H-NMR (300 MHz, CDCl₃/TMS δ (ppm))

2.22 (3H, s), 2.73 (3H, s), 7.37 (2H, d),

7.50 (1H, brs), 8.00 (1H, s), 8.02 (1H, d)

Reference Example 3 Production of 3-acetylthio-4-methylacetoanilide

162 g (654 mmol) of 3-chlorosulfonyl-4-methylacetoanilide was dissolved in 700 ml of acetic acid. Thereto were added 30 g (983 mmol) of red phosphorus and 1.7 g (6.6 mmol) of iodine, followed by stirring for 5 hours under heating and refluxing. The reaction mixture was allowed to cool to room temperature and then filtered through Celite. The filtrate was concentrated under reduced pressure. The residue was dissolved in ethyl acetate. The solution was washed with an aqueous sodium thiosulfate solution and water. The organic phase obtained was dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure to obtain 77.5 g (yield: 53%) of 3-acetylthio-4-methylacetoanilide.

¹H-NMR (300 MHz, CDCl₃/TMS δ (ppm))

2.12 (3H, s), 2.30 (3H, s), 2.43 (3H, s),

7.21-7.28 (2H, m), 7.46 (1H, d), 7.54 (1H, s)

Reference Example 4 Production of 4-methyl-3-mercaptoaniline

77.5 g (347 mmol) of 3-acetylthio-4-methylacetoanilide was suspended in 700 ml of water. Thereto was added 111 g (2,777 mmol) of sodium hydroxide with stirring. The mixture was stirred for 2 hours under heating and refluxing, and then was allowed to cool to room temperature. The mixture was adjusted to pH 5 using an aqueous hydrochloric acid solution (36%) with stirring under ice-cooling. Extraction with ethyl acetate was conducted. The organic phase obtained was dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure to obtain 47.6 g (yield: 99%) of 4-methyl-3-mercaptoaniline.

¹H-NMR (300 MHz, CDCl₃/TMS δ (ppm))

2.21 (3H, s), 3.21 (1H, s), 3.64 (2H, brs),

6.43 (1H, dd), 6.64 (1H, d), 6.92 (1H, d)

Reference Example 5 Production of 4-methyl-3-(2,2,2-trifluoroethylthio)aniline

47.6 g (342 mmol) of 4-methyl-3-mercaptoaniline was dissolved in 500 ml of N,N-dimethylformamide. Thereto was added 71 g (513 mmol) of potassium carbonate, followed by stirring for 1 hour. To the reaction mixture were added 4.8 g (31.1 mmol) of Rongalit and 122 g (582 mmol) of 2,2,2-trifluoroidoethane in this order, followed by stirring overnight at room temperature. Water was added and extraction with ethyl acetate was conducted. The organic phase obtained was washed with a saturated aqueous sodium chloride solution and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure. The crude product obtained was purified by silica gel column chromatography (developing solvent: a mixed solvent of n-hexane:ethyl acetate=10:1), to obtain 63.8 g (yield: 84%) of 4-methyl-3-(2,2,2-trifluoroethylthio)aniline.

¹H-NMR (300 MHz, CDCl₃/TMS δ (ppm))

2.34 (3H, s), 3.37 (2H, q), 3.59 (2H, brs),

6.56 (1H, dd), 6.82 (1H, d), 6.99 (1H, d)

Reference Example 6 Production of 4-chloro-2-fluoro-5-(2,2,2-trifluoroethylthio)phenyl boronic acid

To 180 ml of diethyl ether was dissolved 15.9 g (49.1 mmol) of (5-bromo-4-chloro-2-fluorophenyl)-2,2,2-trifluoroethylsulfide which was produced by a method described in PCT International Publication No. WO 2012/176856, and the mixture was cooled to −70° C. under nitrogen atmosphere. Thereto was dropwise added 30 ml of n-butyllithium (n-hexane solution, 1.64 mol/liter) for 10 minutes. After 5 minutes, a mixed solution obtained by dissolving 5.1 g (49.1 mmol) of trimethyl borate in 10 ml of diethylether was dropwise added in 10 minutes. Then, the temperature of the reaction mixture was raised to −20° C., 48 g of 20% sulfuric acid was dropwise added, and reaction was conducted in a room temperature for 1.5 hour. To the reaction mixture, ethyl acetate was added, the organic phase obtained was washed with water and aqueous sodium chloride solution, and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure and the residue was washed with n-hexane, to obtain 9.64 g (yield: 68%) of an intended product.

¹H-NMR (400 MHz, CDCl₃/TMS δ (ppm))

3.49 (2H, q), 7.30 (1H, d), 8.29 (1H, d)

Reference Example 7 Production of 2,4-dichloro-5-(2,2,2-trifluoroethylthio)phenyl boronic acid

To 700 ml of diethyl ether was dissolved 46.4 g (136 mmol) of (5-bromo-2,4-dichlorophenyl)-2,2,2-trifluoroethylsulfide which was produced by a method described in PCT International Publication No. WO 2012/176856, and the mixture was cooled to −70° C. under nitrogen atmosphere. Thereto was dropwise added 82.7 ml of n-butyllithium (n-hexane solution, 1.64 mol/liter) for 10 minutes. After 5 minutes, a mixed solution obtained by dissolving 14.1 g (136 mmol) of trimethyl borate in 100 ml of diethylether was dropwise added in 10 minutes. Then, the temperature of the reaction mixture was raised to −20° C., 230 ml of 12% (approximately) sulfuric acid was dropwise added, and reaction was conducted in a room temperature for 1.5 hour. The solvent was distilled of under reduced pressure, and to the residue, ethyl acetate was added. The organic phase obtained was washed with water and aqueous sodium chloride solution, and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure and the residue was washed with n-hexane, to obtain 32.58 g (yield: 79%) of an intended product.

¹H-NMR (300 MHz, CDCl₃/TMS δ (ppm))

3.49 (2H, q), 5.34 (2H, s), 7.47 (1H, s), 8.11 (1H, s)

The physical properties (melting point, refractive index, ¹H-NMR spectrum data and specific rotation of optical isomer) of the present compounds [I] and [I′] synthesized based on the Examples (including the physical properties shown in the Examples) are shown in Table 43 to Table 71. Incidentally, the compound Nos. and symbols in Tables have the same meanings as given above.

TABLE 43 Compound No. Physical Property A-0001 Reflactive Index (n_(D) ²⁰) 1.4922 A-0004 Reflactive Index (n_(D) ²⁰) 1.5072 A-0005 Melting Point (° C.) 140-141 A-0006 Reflactive Index (n_(D) ²⁰) 1.4819 A-0007 Melting Point (° C.) 89-92 A-0012 Reflactive Index (n_(D) ²⁰) 1.5055 A-0013 Melting Point (° C.) 87-89 A-0014 Reflactive Index (n_(D) ²⁰) 1.4827 A-0015 Melting Point (° C.) 58-60 A-0017 Reflactive Index (n_(D) ²⁰) 1.5016 A-0018 Melting Point (° C.) 87-88 A-0022 Reflactive Index (n_(D) ²⁰) 1.4893 A-0023 Melting Point (° C.) 53-54 A-0024 Reflactive Index (n_(D) ²⁰) 1.5008 A-0025 Melting Point (° C.) 97-99 A-0027 Reflactive Index (n_(D) ²⁰) 1.4952 A-0028 Melting Point (° C.) 74-76 A-0030 Reflactive Index (n_(D) ²⁰) 1.4800 A-0031 Melting Point (° C.) 64-67 A-0032 Reflactive Index (n_(D) ²⁰) 1.4819 A-0033 Melting Point (° C.) 117-118 A-0035 Reflactive Index (n_(D) ²⁰) 1.5032 A-0036 Melting Point (° C.) 125-127 A-0037 Reflactive Index (n_(D) ²⁰) 1.4810 A-0038 Melting Point (° C.) 77-80 A-0039 Reflactive Index (n_(D) ²⁰) 1.5032 A-0040 Melting Point (° C.) 105-107 A-0043 Reflactive Index (n_(D) ²⁰) 1.4809 A-0044 Melting Point (° C.) 68-70 A-0046 Reflactive Index (n_(D) ²⁰) 1.5004 A-0047 Melting Point (° C.) 97-98 A-0051 Reflactive Index (n_(D) ²⁰) 1.4769 A-0052 Melting Point (° C.) 78-79 A-0055 Reflactive Index (n_(D) ²⁰) 1.4987 A-0056 Melting Point (° C.) 77-79 A-0061 Reflactive Index (n_(D) ²⁰) 1.4900 A-0064 Reflactive Index (n_(D) ²⁰) 1.4989 A-0065 Melting Point (° C.) 106-109 A-0066 Melting Point (° C.) 113-114

TABLE 44 Compound No. Physical Property A-0068 Reflactive Index (n_(D) ²⁰) 1.5011 A-0069 Melting Point (° C.) 138-139 A-0070 Reflactive Index (n_(D) ²⁰) 1.4760 A-0071 Melting Point (° C.)  98-100 A-0074 Reflactive Index (n_(D) ²⁰) 1.4748 A-0075 Melting Point (° C.) 74-75 A-0076 Reflactive Index (n_(D) ²⁰) 1.4830 A-0077 Melting Point (° C.) 65-66 A-0078 Reflactive Index (n_(D) ²⁰) 1.4961 A-0079 Melting Point (° C.) 81-83 A-0081 Reflactive Index (n_(D) ²⁰) 1.4820 A-0085 Reflactive Index (n_(D) ²⁰) 1.4780 A-0086 Melting Point (° C.) 84-85 A-0087 Reflactive Index (n_(D) ²⁰) 1.4915 A-0088 Melting Point (° C.) 62-64 A-0089 Reflactive Index (n_(D) ²⁰) 1.4933 A-0090 Melting Point (° C.) 83-84 A-0091 Reflactive Index (n_(D) ²⁰) 1.4865 A-0092 Melting Point (° C.) 51-52 A-0094 Melting Point (° C.) 108-110 A-0108 Melting Point (° C.) 50-51 A-0109 Melting Point (° C.) 56-57 A-0110 Melting Point (° C.) 76-77 A-0111 Melting Point (° C.) 105-107 A-0112 Reflactive Index (n_(D) ²⁰) 1.5032 A-0113 Melting Point (° C.) 74-75 A-0114 Melting Point (° C.) 76-77 A-0115 Reflactive Index (n_(D) ²⁰) 1.5160 A-0116 Reflactive Index (n_(D) ²⁰) 1.4834 A-0117 Melting Point (° C.) 52-54 A-0118 Reflactive Index (n_(D) ²⁰) 1.4899 A-0119 Melting Point (° C.) 104-105 A-0120 Reflactive Index (n_(D) ²⁰) 1.4790 A-0122 Reflactive Index (n_(D) ²⁰) 1.4790 A-0123 Melting Point (° C.) 58-60 A-0125 Reflactive Index (n_(D) ²⁰) 1.4949 A-0126 Melting Point (° C.) 46-48 A-0130 Melting Point (° C.) 59-60 A-0132 Reflactive Index (n_(D) ²⁰) 1.4842

TABLE 45 Compound No. Physical Property A-0133 Melting Point (° C.) 48-50 A-0141 Melting Point (° C.) 60-61 A-0143 Reflactive Index (n_(D) ²⁰) 1.4871 A-0144 Melting Point (° C.) 47-48 A-0145 Melting Point (° C.) 78-81 A-0147 Reflactive Index (n_(D) ²⁰) 1.4870 A-0157 Melting Point (° C.) 86-88 A-0159 Reflactive Index (n_(D) ²⁰) 1.4542 A-0160 Melting Point (° C.) 100-103 A-0163 Reflactive Index (n_(D) ²⁰) 1.4549 A-0164 Melting Point (° C.) 79-81 A-0167 Reflactive Index (n_(D) ²⁰) 1.4562 A-0168 Melting Point (° C.) 33-35 A-0169 Reflactive Index (n_(D) ²⁰) 1.4631 A-0170 Melting Point (° C.) 44-47 A-0172 Reflactive Index (n_(D) ²⁰) 1.4303 A-0173 Melting Point (° C.) 72-74 A-0174 Reflactive Index (n_(D) ²⁰) 1.4365 A-0175 Melting Point (° C.) 57-59 A-0180 Reflactive Index (n_(D) ²⁰) 1.4429 A-0181 Melting Point (° C.) 94-96 A-0184 Reflactive Index (n_(D) ²⁰) 1.4200 A-0185 Melting Point (° C.) 47-48 A-0186 Reflactive Index (n_(D) ²⁰) 1.4184 A-0187 Melting Point (° C.) 56-58 A-0188 Reflactive Index (n_(D) ²⁰) 1.4445 A-0199 Reflactive Index (n_(D) ²⁰) 1.4554 A-0200 Reflactive Index (n_(D) ²⁰) 1.4613 A-0203 Reflactive Index (n_(D) ²⁰) 1.4562 A-0204 Reflactive Index (n_(D) ²⁰) 1.4644 A-0205 Reflactive Index (n_(D) ²⁰) 1.4678 A-0206 Melting Point (° C.) 39-42 A-0207 Reflactive Index (n_(D) ²⁰) 1.4725 A-0208 Reflactive Index (n_(D) ²⁰) 1.4802 A-0211 Reflactive Index (n_(D) ²⁰) 1.419 A-0212 Reflactive Index (n_(D) ²⁰) 1.4273 A-0213 Reflactive Index (n_(D) ²⁰) 1.4382 A-0214 Reflactive Index (n_(D) ²⁰) 1.4378 A-0215 Reflactive Index (n_(D) ²⁰) 1.4309

TABLE 46 Compound No. Physical Property A-0216 Reflactive Index (n_(D) ²⁰) 1.4341 A-0217 Reflactive Index (n_(D) ²⁰) 1.4341 A-0218 Reflactive Index (n_(D) ²⁰) 1.4359 A-0219 Reflactive Index (n_(D) ²⁰) 1.4200 A-0220 Reflactive Index (n_(D) ²⁰) 1.4321 A-0221 Reflactive Index (n_(D) ²⁰) 1.4368 A-0222 Reflactive Index (n_(D) ²⁰) 1.4401 A-0223 Reflactive Index (n_(D) ²⁰) 1.4328 A-0224 Melting Point (° C.) 45-47 A-0225 Reflactive Index (n_(D) ²⁰) 1.4163 A-0226 Reflactive Index (n_(D) ²⁰) 1.4115 A-0227 Reflactive Index (n_(D) ²⁰) 1.3980 A-0228 Reflactive Index (n_(D) ²⁰) 1.4079 A-0229 Reflactive Index (n_(D) ²⁰) 1.4018 A-0230 Melting Point (° C.) 43-44 A-0232 Reflactive Index (n_(D) ²⁰) 1.3759 A-0243 Reflactive Index (n_(D) ²⁰) 1.4961 A-0244 Melting Point (° C.) 79-80 A-0249 Reflactive Index (n_(D) ²⁰) 1.4947 A-0250 Reflactive Index (n_(D) ²⁰) 1.4929 A-0253 Reflactive Index (n_(D) ²⁰) 1.4751 A-0254 Melting Point (° C.) 116-118 A-0260 Reflactive Index (n_(D) ²⁰) 1.4963 A-0261 Reflactive Index (n_(D) ²⁰) 1.5132 A-0262 Melting Point (° C.) 89-92 A-0263 Reflactive Index (n_(D) ²⁰) 1.5241 A-0264 Reflactive Index (n_(D) ²⁰) 1.5102 A-0266 Reflactive Index (n_(D) ²⁰) 1.5260 A-0269 Reflactive Index (n_(D) ²⁰) 1.5092 A-0270 Melting Point (° C.) 53-55 A-0271 Reflactive Index (n_(D) ²⁰) 1.5078 A-0273 Reflactive Index (n_(D) ²⁰) 1.5211 A-0275 Reflactive Index (n_(D) ²⁰) 1.5133 A-0277 Reflactive Index (n_(D) ²⁰) 1.5195 A-0279 Reflactive Index (n_(D) ²⁰) 1.5160 A-0281 Reflactive Index (n_(D) ²⁰) 1.5071 A-0285 Reflactive Index (n_(D) ²⁰) 1.4981 A-0287 Reflactive Index (n_(D) ²⁰) 1.5206 A-0289 Reflactive Index (n_(D) ²⁰) 1.4943

TABLE 47 Compound No. Physical Property A-0290 Reflactive Index (n_(D) ²⁰) 1.4940 A-0291 Reflactive Index (n_(D) ²⁰) 1.5089 A-0294 Reflactive Index (n_(D) ²⁰) 1.5199 A-0299 Reflactive Index (n_(D) ²⁰) 1.5102 A-0301 Reflactive Index (n_(D) ²⁰) 1.4960 A-0303 Reflactive Index (n_(D) ²⁰) 1.5094 A-0307 Reflactive Index (n_(D) ²⁰) 1.4761 A-0308 Melting Point (° C.) 54-56 A-0311 Reflactive Index (n_(D) ²⁰) 1.4741 A-0313 Melting Point (° C.) 75-78 A-0314 Melting Point (° C.) 93-96 A-0315 Reflactive Index (n_(D) ²⁰) 1.4912 A-0316 Melting Point (° C.) 85-88 A-0318 Melting Point (° C.) 77-80 A-0319 Reflactive Index (n_(D) ²⁰) 1.4851 A-0320 Melting Point (° C.) 116-117 A-0321 Reflactive Index (n_(D) ²⁰) 1.4969 A-0322 Melting Point (° C.) 117-118 A-0324 Reflactive Index (n_(D) ²⁰) 1.4752 A-0325 Reflactive Index (n_(D) ²⁰) 1.4832 A-0326 Melting Point (° C.) 119-122 A-0327 Melting Point (° C.) 92-95 A-0330 Melting Point (° C.) 115-118 A-0331 Melting Point (° C.) 120-121 A-0338 Reflactive Index (n_(D) ²⁰) 1.4751 A-0339 Reflactive Index (n_(D) ²⁰) 1.4798 A-0340 Reflactive Index (n_(D) ²⁰) 1.4831 A-0341 Reflactive Index (n_(D) ²⁰) 1.4859 A-0342 Reflactive Index (n_(D) ²⁰) 1.4968 A-0343 Melting Point (° C.) 66-67 A-0346 Reflactive Index (n_(D) ²⁰) 1.4950 A-0347 Melting Point (° C.) 89-90 A-0349 Reflactive Index (n_(D) ²⁰) 1.5321 A-0350 Melting Point (° C.) 117-118 A-0352 Melting Point (° C.) 83-84 A-0353 Melting Point (° C.) 51-52 A-0354 Melting Point (° C.) 88-90 A-0356 Melting Point (° C.) 54-56 A-0359 Melting Point (° C.) 74-77

TABLE 48 Compound No. Physical Property A-0360 Reflactive Index (n_(D) ²⁰) 1.5079 A-0363 Reflactive Index (n_(D) ²⁰) 1.5012 A-0364 Melting Point (° C.) 46-47 A-0365 Reflactive Index (n_(D) ²⁰) 1.5104 A-0366 Melting Point (° C.) 42-43 A-0368 Melting Point (° C.) 69-71 A-0369 Reflactive Index (n_(D) ²⁰) 1.5089 A-0374 Reflactive Index (n_(D) ²⁰) 1.4990 A-0375 Melting Point (° C.) 48-50 A-0379 Reflactive Index (n_(D) ²⁰) 1.5217 A-0387 Melting Point (° C.) 68-70 A-0388 Melting Point (° C.) 111-112 A-0391 Melting Point (° C.) 88-89 A-0392 Melting Point (° C.) 95-98 A-0393 Melting Point (° C.) 98-99 A-0394 Melting Point (° C.) 109-110 A-0395 Melting Point (° C.) 93-94 A-0396 Melting Point (° C.) 108-109 A-0405 Reflactive Index (n_(D) ²⁰) 1.4741 A-0406 Reflactive Index (n_(D) ²⁰) 1.4800 A-0415 Reflactive Index (n_(D) ²⁰) 1.4762 A-0417 Reflactive Index (n_(D) ²⁰) 1.4882 A-0418 Melting Point (° C.) 57-59 A-0422 Reflactive Index (n_(D) ²⁰) 1.4855 A-0423 Reflactive Index (n_(D) ²⁰) 1.4869 A-0431 Reflactive Index (n_(D) ²⁰) 1.4742 A-0433 Reflactive Index (n_(D) ²⁰) 1.4932 A-0434 Melting Point (° C.) 49-50 A-0435 Melting Point (° C.) 51-52 A-0437 Reflactive Index (n_(D) ²⁰) 1.5000 A-0438 Reflactive Index (n_(D) ²⁰) 1.4878 A-0439 Reflactive Index (n_(D) ²⁰) 1.4889 A-0441 Melting Point (° C.) 68-69 A-0443 Melting Point (° C.) 41-42 A-0444 Reflactive Index (n_(D) ²⁰) 1.5006 A-0445 Melting Point (° C.) 63-66 A-0446 Reflactive Index (n_(D) ²⁰) 1.4947 A-0447 Reflactive Index (n_(D) ²⁰) 1.4931 A-0448 Reflactive Index (n_(D) ²⁰) 1.4781

TABLE 49 Compound No. Physical Property A-0449 Melting Point (° C.) 69-70 A-0470 Reflactive Index (n_(D) ²⁰) 1.4770 A-0471 Melting Point (° C.) 42-44 A-0472 Reflactive Index (n_(D) ²⁰) 1.4905 A-0473 Melting Point (° C.) 43-46 A-0474 Reflactive Index (n_(D) ²⁰) 1.4886 A-0475 Reflactive Index (n_(D) ²⁰) 1.4862 A-0476 Reflactive Index (n_(D) ²⁰) 1.4951 A-0477 Melting Point (° C.) 45-48 A-0478 Reflactive Index (n_(D) ²⁰) 1.5059 A-0479 Melting Point (° C.) 43-45 A-0481 Reflactive Index (n_(D) ²⁰) 1.4859 A-0482 Reflactive Index (n_(D) ²⁰) 1.4960 A-0483 Reflactive Index (n_(D) ²⁰) 1.491 A-0484 Reflactive Index (n_(D) ²⁰) 1.4759 A-0485 Reflactive Index (n_(D) ²⁰) 1.4800 A-0486 Reflactive Index (n_(D) ²⁰) 1.5086 A-0487 Reflactive Index (n_(D) ²⁰) 1.5102 A-0488 Reflactive Index (n_(D) ²⁰) 1.5005 A-0489 Reflactive Index (n_(D) ²⁰) 1.4978 A-0490 Reflactive Index (n_(D) ²⁰) 1.5181 A-0495 Reflactive Index (n_(D) ²⁰) 1.4839 A-0496 Reflactive Index (n_(D) ²⁰) 1.4782 A-0502 Reflactive Index (n_(D) ²⁰) 1.4813 A-0503 Reflactive Index (n_(D) ²⁰) 1.4773 A-0504 Reflactive Index (n_(D) ²⁰) 1.4814 A-0505 Melting Point (° C.) 48-49 A-0507 Reflactive Index (n_(D) ²⁰) 1.4932 A-0508 Melting Point (° C.) 43-44 A-0510 Melting Point (° C.) 44-45 A-0524 Melting Point (° C.) 82-83 A-0525 Melting Point (° C.) 50-51 A-0526 Reflactive Index (n_(D) ²⁰) 1.4920 A-0533 Melting Point (° C.) 80-81 A-0534 Melting Point (° C.) 92-93 A-0535 Reflactive Index (n_(D) ²⁰) 1.4709 A-0536 Melting Point (° C.) 73-74 A-0539 Melting Point (° C.) 74-77 A-0543 Reflactive Index (n_(D) ²⁰) 1.4949

TABLE 50 Compound No. Physical Property A-0553 Reflactive Index (n_(D) ²⁰) 1.4914 A-0555 Reflactive Index (n_(D) ²⁰) 1.5025 A-0556 Melting Point (° C.) 40-42 A-0558 Reflactive Index (n_(D) ²⁰) 1.5052 A-0559 Reflactive Index (n_(D) ²⁰) 1.5125 A-0560 Melting Point (° C.) 49-50 A-0561 Reflactive Index (n_(D) ²⁰) 1.5201 A-0562 Melting Point (° C.) 57-59 A-0563 Reflactive Index (n_(D) ²⁰) 1.5025 A-0571 Reflactive Index (n_(D) ²⁰) 1.4957 A-0572 Reflactive Index (n_(D) ²⁰) 1.5000 A-0573 Reflactive Index (n_(D) ²⁰) 1.5023 A-0574 Reflactive Index (n_(D) ²⁰) 1.4982 A-0575 Reflactive Index (n_(D) ²⁰) 1.5098 A-0576 Reflactive Index (n_(D) ²⁰) 1.5087 A-0577 Melting Point (° C.) 68-69 A-0578 Melting Point (° C.) 58-59 A-0587 Reflactive Index (n_(D) ²⁰) 1.4941 A-0588 Reflactive Index (n_(D) ²⁰) 1.4981 A-0589 Reflactive Index (n_(D) ²⁰) 1.5010 A-0590 Melting Point (° C.) 41-42 A-0591 Melting Point (° C.) 50-51 A-0592 Reflactive Index (n_(D) ²⁰) 1.5000 A-0594 Melting Point (° C.) 112-113 A-0599 Melting Point (° C.) 65-67 A-0605 Melting Point (° C.) 87-90 A-0606 Melting Point (° C.) 78-81 A-0610 Reflactive Index (n_(D) ²⁰) 1.4909 A-0611 Melting Point (° C.) 96-99 A-0615 Melting Point (° C.) 60-61 A-0616 Melting Point CO 58-60 A-0617 Melting Point (° C.) 38-41 A-0618 Melting Point (° C.) 82-83 A-0622 Reflactive Index (n_(D) ²⁰) 1.4864 A-0623 Melting Point (° C.) 86-88 A-0625 Reflactive Index (n_(D) ²⁰) 1.4861 A-0626 Reflactive Index (n_(D) ²⁰) 1.4899 A-0631 Reflactive Index (n_(D) ²⁰) 1.4845 A-0632 Melting Point (° C.) 72-74

TABLE 51 Compound No. Physical Property A-0638 Melting Point (° C.) 39-41 A-0640 Reflactive Index (n_(D) ²⁰) 1.4902 A-0641 Melting Point (° C.) 68-69 A-0642 Melting Point (° C.) 43-44 A-0643 Melting Point (° C.) 61-63 A-0644 Reflactive Index (n_(D) ²⁰) 1.5000 A-0662 Reflactive Index (n_(D) ²⁰) 1.5353 A-0663 Reflactive Index (n_(D) ²⁰) 1.5190 A-0665 Reflactive Index (n_(D) ²⁰) 1.5309 A-0666 Reflactive Index (n_(D) ²⁰) 1.5272 A-0667 Reflactive Index (n_(D) ²⁰) 1.5509 A-0668 Reflactive Index (n_(D) ²⁰) 1.5155 A-0670 Reflactive Index (n_(D) ²⁰) 1.5281 A-0671 Reflactive Index (n_(D) ²⁰) 1.5325 A-0672 Reflactive Index (n_(D) ²⁰) 1.5299 A-0673 Reflactive Index (n_(D) ²⁰) 1.5161 A-0674 Reflactive Index (n_(D) ²⁰) 1.5130 A-0675 Reflactive Index (n_(D) ²⁰) 1.5122 A-0676 Reflactive Index (n_(D) ²⁰) 1.5210 A-0677 Reflactive Index (n_(D) ²⁰) 1.5240 A-0680 Reflactive Index (n_(D) ²⁰) 1.5085 A-0682 Reflactive Index (n_(D) ²⁰) 1.5121 A-0683 Reflactive Index (n_(D) ²⁰) 1.4769 A-0684 Reflactive Index (n_(D) ²⁰) 1.5361 A-0686 Melting Point (° C.) 108-110 A-0688 Melting Point (° C.) 111-112 A-0690 Reflactive Index (n_(D) ²⁰) 1.5016 A-0692 Melting Point (° C.) 81-83 A-0693 Reflactive Index (n_(D) ²⁰) 1.5092 A-0694 Melting Point (° C.) 86-87 A-0695 Melting Point (° C.) 39-41 A-0696 Melting Point (° C.) 125-127 A-0697 Melting Point (° C.) 102-104 A-0698 Melting Point (° C.) 113-116 A-0699 Melting Point (° C.) 53-55 A-0700 Melting Point (° C.) 112-114 A-0703 Melting Point (° C.) 63-64 A-0709 Melting Point (° C.) 59-60 A-0710 Melting Point (° C.)  98-100

TABLE 52 Compound No. Physical Property A-0711 Melting Point (° C.) 61-63 A-0712 Melting Point (° C.) 89-90 A-0713 Reflactive Index (n_(D) ²⁰) 1.5188 A-0716 Melting Point (° C.) 66-68 A-0717 Melting Point (° C.) 80-81 A-0718 Melting Point (° C.) 79-82 A-0720 Reflactive Index (n_(D) ²⁰) 1.5330 A-0721 Melting Point (° C.) 128-129 A-0722 Melting Point (° C.) 50-51 A-0723 Melting Point (° C.) 90-91 A-0724 Melting Point (° C.) 96-97 A-0725 Melting Point (° C.) 144-145 A-0726 Melting Point (° C.) 117-119 A-0727 Melting Point (° C.) 93-96 A-0728 Melting Point (° C.)   47-48.5 A-0729 Melting Point (° C.) 117-118 A-0730 Melting Point (° C.) 70-71 A-0731 Melting Point (° C.) 125-126 A-0732 Reflactive Index (n_(D) ²⁰) 1.5021 A-0733 Melting Point (° C.) 144-145 A-0734 Reflactive Index (n_(D) ²⁰) 1.5072 A-0735 Melting Point (° C.) 132-134 A-0736 Melting Point (° C.) 122-123 A-0739 Melting Point (° C.) 79-80 A-0740 Melting Point (° C.) 138-140 A-0741 Melting Point (° C.) 52-53 A-0742 Melting Point (° C.) 114-116 A-0743 Melting Point (° C.) 52-53 A-0744 Melting Point (° C.) 103-104 A-0746 Melting Point (° C.) 101-102 A-0748 Reflactive Index (n_(D) ²⁰) 1.4766 A-0749 Melting Point (° C.) 96-98 A-0750 Melting Point (° C.) 85-87 A-0751 Reflactive Index (n_(D) ²⁰) 1.5319 A-0752 Melting Point (° C.) 78-80 A-0753 Reflactive Index (n_(D) ²⁰) 1.5224 A-0754 Melting Point (° C.) 92-94 A-0755 Reflactive Index (n_(D) ²⁰) 1.5279 A-0756 Melting Point (° C.) 102-103

TABLE 53 Compound No. Physical Property A-0757 Reflactive Index(n_(D) ²⁰) 1.5500 A-0758 Melting Point (° C.) 104-105 A-0759 Reflactive Index (n_(D) ²⁰) 1.5030 A-0760 Melting Point (° C.) 125-128 A-0761 Reflactive Index (n_(D) ²⁰) 1.4979 A-0762 Reflactive Index (n_(D) ²⁰) 1.5050 A-0763 Reflactive Index (n_(D) ²⁰) 1.4991 A-0764 Melting Point (° C.) 95-96 A-0765 Reflactive Index (n_(D) ²⁰) 1.5085 A-0766 Melting Point (° C.) 91-92 A-0767 Melting Point (° C.) 109-110 A-0768 Melting Point (° C.) 91-92 A-0769 Melting Point (° C.) 115-116 A-0771 Melting Point (° C.) 115-116 A-0772 Reflactive Index (n_(D) ²⁰) 1.5190 A-0773 Melting Point (° C.) 89-90 A-0774 Melting Point (° C.) 75-76 A-0775 Melting Point (° C.) 81-82 A-0776 Melting Point (° C.) 118-120 A-0777 Melting Point (° C.) 40-41 A-0778 Reflactive Index (n_(D) ²⁰) 1.4976 A-0779 Melting Point (° C.) 81-84 A-0780 Reflactive Index (n_(D) ²⁰) 1.5009 A-0781 Melting Point (° C.) 94-95 A-0782 Melting Point (° C.) 111-112 A-0783 Melting Point (° C.) 80-81 A-0784 Melting Point (° C.) 120-122 A-0786 Reflactive Index (n_(D) ²⁰) 1.5158 A-0787 Reflactive Index (n_(D) ²⁰) 1.5247 A-0788 Melting Point (° C.) 89-90 A-0789 Melting Point (° C.) 114-115 A-0790 Melting Point (° C.) 51-54 A-0791 Melting Point (° C.) 131-134 A-0792 Melting Point (° C.) 110-111 A-0793 Melting Point (° C.) 126-127 A-0795 Melting Point (° C.) 117-118 A-0796 Melting Point (° C.) 133-136 A-0797 Reflactive Index (n_(D) ²⁰) 1.5062 A-0798 Reflactive Index (n_(D) ²⁰) 1.4980

TABLE 54 Compound No. Physical Property A-0799 Melting Point (° C.) 79-81 A-0800 Melting Point (° C.) 83-84 A-0801 Melting Point (° C.) 109-110 A-0802 Reflactive Index (n_(D) ²⁰) 1.5540 A-0803 Melting Point (° C.) 135-136 A-0805 Melting Point (° C.) 92-93 A-0806 Melting Point (° C.) 101-102 A-0807 Melting Point (° C.) 115-116 A-0808 Melting Point (° C.) 106-109 A-0809 Reflactive Index (n_(D) ²⁰) 1.5051 A-0810 Melting Point (° C.) 88-90 A-0811 Reflactive Index (n_(D) ²⁰) 1.5021 A-0812 Melting Point (° C.) 107-109 A-0813 Reflactive Index (n_(D) ²⁰) 1.4896 A-0814 Melting Point (° C.) 104-106 A-0815 Reflactive Index (n_(D) ²⁰) 1.4987 A-0816 Melting Point (° C.) 111-112 A-0817 Melting Point (° C.)  98-100 A-0818 Melting Point (° C.) 86-88 A-0819 Reflactive Index (n_(D) ²⁰) 1.5210 A-0820 Melting Point (° C.) 99-100 A-0821 Melting Point (° C.) 90-91 A-0823 Melting Point (° C.) 93-95 A-0824 Reflactive Index (n_(D) ²⁰) 1.5005 A-0825 Melting Point (° C.) 72-73 A-0826 Reflactive Index (n_(D) ²⁰) 1.5282 A-0827 Melting Point (° C.) 76-78 A-0828 Reflactive Index (n_(D) ²⁰) 1.5463 A-0829 Melting Point (° C.) 144-145 A-0830 Reflactive Index (n_(D) ²⁰) 1.5589 A-0831 Reflactive Index (n_(D) ²⁰) 1.5479 A-0832 Reflactive Index (n_(D) ²⁰) 1.5406 A-0833 Melting Point (° C.) 49-52 A-0837 Melting Point (° C.) 96-97 A-0838 Reflactive Index (n_(D) ²⁰) 1.4970 A-0839 Melting Point (° C.) 101-102 A-0844 Reflactive Index (n_(D) ²⁰) 1.4962 A-0845 Reflactive Index (n_(D) ²⁰) 1.5025 A-0846 Reflactive Index (n_(D) ²⁰) 1.5270

TABLE 55 Compound No. Physical Property A-0847 Melting Point (° C.) 58-60 A-0848 Reflactive Index (n_(D) ²⁰) 1.5382 A-0849 Melting Point (° C.) 92-94 A-0853 Reflactive Index (n_(D) ²⁰) 1.5140 A-0854 Melting Point (° C.) 100-103 A-0855 Reflactive Index (n_(D) ²⁰) 1.5028 A-0856 Melting Point (° C.)  98-100 A-0857 Reflactive Index (n_(D) ²⁰) 1.4969 A-0858 Melting Point (° C.) 101-102 A-0860 Reflactive Index (n_(D) ²⁰) 1.5256 A-0864 Melting Point (° C.) 87-88 A-0869 Reflactive Index (n_(D) ²⁰) 1.5241 A-0870 Reflactive Index (n_(D) ²⁰) 1.5207 A-0876 Melting Point (° C.) 82-84 A-0877 Reflactive Index (n_(D) ²⁰) 1.5442 A-0878 Melting Point (° C.) 44-46 A-0880 Reflactive Index (n_(D) ²⁰) 1.5235 A-0881 Melting Point (° C.) 69-72 A-0884 Reflactive Index (n_(D) ²⁰) 1.5201 A-0885 Melting Point (° C.) 49-50 A-0888 Reflactive Index (n_(D) ²⁰) 1.5602 A-0902 Reflactive Index (n_(D) ²⁰) 1.5450 A-0903 Melting Point (° C.) 83-85 A-0906 Melting Point (° C.) 140-143 A-0907 Reflactive Index (n_(D) ²⁰) 1.5382 A-0908 Reflactive Index (n_(D) ²⁰) 1.5508 A-0909 Melting Point (° C.) 103-105 A-0913 Reflactive Index (n_(D) ²⁰) 1.5486 A-0914 Reflactive Index (n_(D) ²⁰) 1.5580 A-0915 Reflactive Index (n_(D) ²⁰) 1.5679 A-0916 Reflactive Index (n_(D) ²⁰) 1.5649 A-0917 Reflactive Index (n_(D) ²⁰) 1.5578 A-0918 Reflactive Index (n_(D) ²⁰) 1.5500 A-0919 Reflactive Index (n_(D) ²⁰) 1.5552 A-0920 Reflactive Index (n_(D) ²⁰) 1.5539 A-0921 Reflactive Index (n_(D) ²⁰) 1.5549 A-0922 Melting Point (° C.) 75-77 A-0923 Reflactive Index (n_(D) ²⁰) 1.5171 A-0924 Melting Point (° C.) 83-86

TABLE 56 Compound No. Physical Property A-0925 Melting Point (° C.) 75-76 A-0926 Reflactive Index (n_(D) ²⁰) 1.5667 A-0927 Melting Point (° C.) 75-76 A-0933 Reflactive Index(n_(D) ²⁰) 1.5471 A-0936 Reflactive Index (n_(D) ²⁰) 1.5411 A-0940 Melting Point (° C.) 71-72 A-0941 Reflactive Index (n_(D) ²⁰) 1.5259 A-0942 Melting Point (° C.) 112-114 A-0943 Melting Point (° C.) 93-96 A-0948 Melting Point (° C.) 57-58 A-0950 Melting Point (° C.) 136-138 A-0956 Reflactive Index (n_(D) ²⁰) 1.5046 A-0957 Melting Point (° C.) 94-95 A-0958 Melting Point (° C.) 49-50 A-0959 Reflactive Index (n_(D) ²⁰) 1.4908 A-0960 Melting Point (° C.) 91-92 A-0963 Reflactive Index (n_(D) ²⁰) 1.5309 A-0964 Reflactive Index (n_(D) ²⁰) 1.5341 A-0965 Reflactive Index (n_(D) ²⁰) 1.5219 A-0966 Reflactive Index (n_(D) ²⁰) 1.5269 A-0968 Reflactive Index (n_(D) ²⁰) 1.5635 A-0969 Melting Point (° C.) 93-94 A-0972 Reflactive Index (n_(D) ²⁰) 1.4600 A-0973 Melting Point (° C.) 71-74 A-0975 Reflactive Index (n_(D) ²⁰) 1.5613 A-0976 Melting Point (° C.) 50-51 A-0977 Reflactive Index (n_(D) ²⁰) 1.4741 A-0978 Melting Point (° C.) 85-87 A-0979 Reflactive Index (n_(D) ²⁰) 1.5143 A-0980 Melting Point (° C.) 76-77 A-0981 Reflactive Index (n_(D) ²⁰) 1.4626 A-0982 Melting Point (° C.) 50-53 A-0983 Reflactive Index (n_(D) ²⁰) 1.5621 A-0984 Reflactive Index (n_(D) ²⁰) 1.4711 A-0985 Melting Point (° C.) 66-69 A-0988 Melting Point (° C.) 76-77 A-0989 Reflactive Index (n_(D) ²⁰) 1.5024 A-0990 Melting Point (° C.) 62-63 A-0991 Reflactive Index (n_(D) ²⁰) 1.4639

TABLE 57 Compound No. Physical Property A-0992 Melting Point (° C.) 35-37 A-0996 Melting Point (° C.) 48-51 A-0997 Melting Point (° C.) 55-58 A-0999 Melting Point (° C.) 87-88 A-1000 Melting Point (° C.) 104-105 A-1001 Melting Point (° C.) 91-92 A-1002 Melting Point (° C.) 70-73 A-1003 Reflactive Index (n_(D) ²⁰) 1.5103 A-1004 Reflactive Index (n_(D) ²⁰) 1.5094 A-1005 Melting Point (° C.) 86-88 A-1006 Melting Point (° C.) 72-75 A-1007 Reflactive Index (n_(D) ²⁰) 1.5254 A-1008 Melting Point (° C.) 87-88 A-1009 Reflactive Index (n_(D) ²⁰) 1.5101 A-1010 Melting Point (° C.) 78-80 A-1011 Reflactive Index (n_(D) ²⁰) 1.5272 A-1012 Melting Point (° C.) 91-92 A-1015 Reflactive Index (n_(D) ²⁰) 1.5226 A-1016 Melting Point (° C.) 92-94 A-1020 Reflactive Index (n_(D) ²⁰) 1.4900 A-1021 Melting Point (° C.) 105-108 A-1024 Reflactive Index (n_(D) ²⁰) 1.4931 A-1025 Reflactive Index (n_(D) ²⁰) 1.4852 A-1026 Melting Point (° C.) 71-72 A-1027 Reflactive Index (n_(D) ²⁰) 1.5430 A-1033 Reflactive Index (n_(D) ²⁰) 1.4935 A-1037 Reflactive Index (n_(D) ²⁰) 1.4792 A-1042 Reflactive Index (n_(D) ²⁰) 1.4862 A-1048 Melting Point (° C.) 60-61 A-1050 Reflactive Index (n_(D) ²⁰) 1.4850 A-1051 Reflactive Index (n_(D) ²⁰) 1.4780 A-1052 Reflactive Index (n_(D) ²⁰) 1.4802 A-1057 Reflactive Index (n_(D) ²⁰) 1.4790 A-1058 Reflactive Index (n_(D) ²⁰) 1.4859 A-1059 Melting Point (° C.) 63-64 A-1060 Melting Point (° C.) 75-76 A-1061 Reflactive Index (n_(D) ²⁰) 1.4909 A-1062 Reflactive Index (n_(D) ²⁰) 1.4942 A-1073 Melting Point (° C.) 67-70

TABLE 58 Compound No. Physical Property A-1074 Reflactive Index (n_(D) ²⁰) 1.4919 A-1075 Melting Point (° C.)  82-83 A-1079 Melting Point (° C.)  81-83 A-1080 Melting Point (° C.) 119-122 A-1081 Melting Point (° C.) 101-102 A-1082 Melting Point (° C.) 144-147 A-1087 Reflactive Index (n_(D) ²⁰) 1.4991 A-1088 Melting Point (° C.)  89-92 A-1093 Reflactive Index (n_(D) ²⁰) 1.5029 A-1094 Melting Point (° C.)  99-102 A-1097 Reflactive Index (n_(D) ²⁰) 1.523 A-1098 Melting Point (° C.) 115-117 A-1099 Reflactive Index (n_(D) ²⁰) 1.4985 A-1100 Reflactive Index (n_(D) ²⁰) 1.5051 A-1102 Reflactive Index (n_(D) ²⁰) 1.5152 A-1107 Melting Point (° C.)  92-93 A-1108 Melting Point (° C.) 142-143 A-1112 Reflactive Index (n_(D) ²⁰) 1.4958 A-1113 Melting Point (° C.) 109-111 A-1117 Melting Point (° C.)  94-96 A-1119 Melting Point (° C.) 135-136 A-1122 Melting Point (° C.) 110-113 A-1123 Melting Point (° C.) 117-118 A-1125 Reflactive Index (n_(D) ²⁰) 1.4881 A-1126 Melting Point (° C.)  70-72 A-1127 Reflactive Index (n_(D) ²⁰) 1.5111 A-1128 Reflactive Index (n_(D) ²⁰) 1.5049 A-1131 Melting Point (° C.)  70-73 A-1132 Melting Point (° C.)  70-73 A-1136 Reflactive Index (n_(D) ²⁰) 1.4550 A-1137 Melting Point (° C.)  87-90 A-1138 Reflactive Index (n_(D) ²⁰) 1.4826 A-1139 Melting Point (° C.)  98-101 A-1140 Reflactive Index (n_(D) ²⁰) 1.4622 A-1141 Reflactive Index (n_(D) ²⁰) 1.4682 A-1142 Reflactive Index (n_(D) ²⁰) 1.4750 A-1143 Melting Point (° C.)  85-87 A-1150 Melting Point (° C.) 116-117 A-1151 Melting Point (° C.)  51-52

TABLE 59 Compound No. Physical Property A-1152 Melting Point (° C.) 105-106 A-1153 Melting Point (° C.) 147-148 A-1154 Melting Point (° C.)  89-92 A-1155 Melting Point (° C.)  92-93 A-1157 Melting Point (° C.)  77-80 A-1158 Reflactive Index (n_(D) ²⁰) 1.4679 A-1159 Reflactive Index (n_(D) ²⁰) 1.4715 A-1164 Melting Point (° C.)  62-63 A-1165 Melting Point (° C.)  65-67 A-1166 Reflactive Index (n_(D) ²⁰) 1.4919 A-1167 Melting Point (° C.)  67-68 A-1171 Reflactive Index (n_(D) ²⁰) 1.5335 A-1172 Melting Point (° C.)  99-100 A-1174 Melting Point (° C.) 103-106 A-1175 Reflactive Index (n_(D) ²⁰) 1.4721 A-1177 Reflactive Index (n_(D) ²⁰) 1.4755 A-1178 Melting Point (° C.)  84-87 A-1180 Reflactive Index (n_(D) ²⁰) 1.4729 A-1181 Reflactive Index (n_(D) ²⁰) 1.4730 A-1183 Melting Point (° C.)  79-82 A-1185 Reflactive Index (n_(D) ²⁰) 1.4685 A-1186 Melting Point (° C.) 107-108 A-1187 Melting Point (° C.) 105-107 A-1188 Melting Point (° C.)  84-85 A-1190 Reflactive Index (n_(D) ²⁰) 1.4729 A-1191 Melting Point (° C.) 104-106 A-1192 Melting Point (° C.)  80-81 A-1195 Reflactive Index (n_(D) ²⁰) 1.4720 A-1196 Melting Point (° C.)  90-91 A-1197 Reflactive Index (n_(D) ²⁰) 1.4812 A-1200 Melting Point (° C.) 102-104 A-1202 Melting Point (° C.)  58-61 A-1203 Melting Point (° C.)  89-90 A-1205 Reflactive Index (n_(D) ²⁰) 1.4801 A-1206 Reflactive Index (n_(D) ²⁰) 1.4899 A-1207 Melting Point (° C.)  67-70 A-1209 Reflactive Index (n_(D) ²⁰) 1.4925 A-1210 Reflactive Index (n_(D) ²⁰) 1.4804 A-1211 Melting Point (° C.)  71-72

TABLE 60 Compound No. Physical Property A-1212 Reflactive Index (n_(D) ²⁰) 1.4880 A-1213 Melting Point (° C.) 46-48 A-1214 Melting Point (° C.) 99-100 A-1215 Reflactive Index (n_(D) ²⁰) 1.5418 A-1216 Reflactive Index (n_(D) ²⁰) 1.5391 A-1217 Melting Point (° C.) 69-70 A-1218 Melting Point (° C.) 80-82

TABLE 61 Compound No. Physical Property B-0001 Reflactive Index (n_(D) ²⁰) 1.4980 B-0002 Melting Point (° C.) 116-117 B-0003 Reflactive Index (n_(D) ²⁰) 1.4599 B-0004 Reflactive Index (n_(D) ²⁰) 1.4638 B-0005 Reflactive Index (n_(D) ²⁰) 1.4830 B-0006 Reflactive Index (n_(D) ²⁰) 1.4896 B-0007 Reflactive Index (n_(D) ²⁰) 1.4839 B-0008 Reflactive Index (n_(D) ²⁰) 1.4885 B-0009 Reflactive Index (n_(D) ²⁰) 1.4880 B-0010 Reflactive Index (n_(D) ²⁰) 1.4928 B-0011 Melting Point (° C.)  75-76 B-0012 Reflactive Index (n_(D) ²⁰) 1.5291 B-0013 Melting Point (° C.) 102-103 B-0014 Reflactive Index (n_(D) ²⁰) 1.5534 B-0015 Melting Point (° C.) 103-106 B-0016 Reflactive Index (n_(D) ²⁰) 1.5528 B-0017 Reflactive Index (n_(D) ²⁰) 1.5019 B-0018 Melting Point (° C.)  64-65 B-0019 Melting Point (° C.)  67-68 B-0020 Reflactive Index (n_(D) ²⁰) 1.4952 B-0021 Melting Point (° C.) 124-126 B-0022 Reflactive Index (n_(D) ²⁰) 1.4835 B-0023 Melting Point (° C.)  88-89 B-0024 Reflactive Index (n_(D) ²⁰) 1.5051 B-0025 Melting Point (° C.)  85-86 B-0026 Melting Point (° C.)  57-59 B-0027 Melting Point (° C.)  53-54 B-0029 Reflactive Index (n_(D) ²⁰) 1.5390 B-0030 Melting Point (° C.)  88-91 B-0032 Melting Point (° C.) 117-118 B-0033 Melting Point (° C.)  90-92 B-0034 Melting Point (° C.) 104-107 B-0035 Reflactive Index (n_(D) ²⁰) 1.5013 B-0036 Reflactive Index (n_(D) ²⁰) 1.5145 B-0037 Melting Point (° C.)  94-96 B-0038 Reflactive Index (n_(D) ²⁰) 1.5028 B-0039 Melting Point (° C.)  73-74 B-0040 Melting Point (° C.)  93-95 B-0041 Melting Point (° C.)  85-87

TABLE 62 Compound No. Physical Property B-0042 Reflactive Index (n_(D) ²⁰) 1.5040 B-0043 Reflactive Index (n_(D) ²⁰) 1.5220 B-0044 Melting Point (° C.)  87-89 B-0045 Reflactive Index (n_(D) ²⁰) 1.5168 B-0046 Melting Point (° C.) 114-115 B-0047 Melting Point (° C.) 130-133 B-0048 Melting Point (° C.)  54-56 B-0049 Melting Point (° C.) 124-125 B-0050 Melting Point (° C.) 133-134 B-0051 Reflactive Index (n_(D) ²⁰) 1.4976 B-0052 Melting Point (° C.) 147-149 B-0053 Melting Point (° C.)  54-55 B-0054 Melting Point (° C.) 117-118 B-0055 Reflactive Index (n_(D) ²⁰) 1.5098 B-0056 Melting Point (° C.)  74-75 B-0058 Melting Point (° C.)  94-96 B-0059 Melting Point (° C.)  74-77 B-0061 Melting Point (° C.) 108-109 B-0062 Melting Point (° C.)  99-101 B-0064 Reflactive Index (n_(D) ²⁰) 1.5210 B-0065 Melting Point (° C.) 142-144 B-0066 Reflactive Index (n_(D) ²⁰) 1.5059 B-0067 Melting Point (° C.)  94-96 B-0068 Reflactive Index (n_(D) ²⁰) 1.5085 B-0069 Melting Point (° C.) 126-127 B-0070 Reflactive Index (n_(D) ²⁰) 1.4985 B-0071 Melting Point (° C.) 109-110 B-0072 Reflactive Index (n_(D) ²⁰) 1.5031 B-0073 Melting Point (° C.)  78-79 B-0074 Reflactive Index (n_(D) ²⁰) 1.4950 B-0075 Melting Point (° C.) 104-105 B-0076 Reflactive Index (n_(D) ²⁰) 1.4970 B-0077 Melting Point (° C.)  77-78 B-0078 Reflactive Index (n_(D) ²⁰) 1.4955 B-0079 Melting Point (° C.)  83-85 B-0080 Reflactive Index (n_(D) ²⁰) 1.5051 B-0081 Melting Point (° C.)  68-69 B-0082 Reflactive Index (n_(D) ²⁰) 1.4904 B-0083 Melting Point (° C.)  69-70

TABLE 63 Compound No. Physical Property B-0084 Reflactive Index (n_(D) ²⁰) 1.4713 B-0085 Melting Point (° C.)  92-94 B-0086 Reflactive Index (n_(D) ²⁰) 1.4638 B-0087 Melting Point (° C.)  98-100 B-0088 Reflactive Index (n_(D) ²⁰) 1.4912 B-0089 Melting Point (° C.) 115-117 B-0090 Reflactive Index (n_(D) ²⁰) 1.5022 B-0091 Melting Point (° C.) 106-108 B-0092 Reflactive Index (n_(D) ²⁰) 1.5005 B-0093 Reflactive Index (n_(D) ²⁰) 1.4921 B-0094 Reflactive Index (n_(D) ²⁰) 1.5022 B-0095 Melting Point (° C.) 106-108 B-0096 Melting Point (° C.)  57-58 B-0097 Reflactive Index (n_(D) ²⁰) 1.5038 B-0098 Melting Point (° C.)  63-65 B-0099 Reflactive Index (n_(D) ²⁰) 1.5042 B-0100 Melting Point (° C.) 110-111 B-0101 Reflactive Index (n_(D) ²⁰) 1.5440 B-0102 Reflactive Index (n_(D) ²⁰) 1.5120 B-0103 Melting Point (° C.) 117-118 B-0104 Reflactive Index (n_(D) ²⁰) 1.5057 B-0105 Melting Point (° C.) 104-106 B-0106 Reflactive Index (n_(D) ²⁰) 1.5441 B-0107 Reflactive Index (n_(D) ²⁰) 1.5428 B-0108 Reflactive Index (n_(D) ²⁰) 1.4988 B-0109 Reflactive Index (n_(D) ²⁰) 1.5384 B-0113 Reflactive Index (n_(D) ²⁰) 1.5578 B-0114 Melting Point (° C.)  89-100 B-0115 Melting Point (° C.)  86-89 B-0116 Melting Point (° C.) 114-115 B-0117 Melting Point (° C.)  84-85

TABLE 64 Compound No. Physical Property C-0001 Reflactive Index (n_(D) ²⁰) 1.4915 C-0002 Melting Point (° C.) 174-177 C-0003 Reflactive Index (n_(D) ²⁰) 1.5185 C-0004 Melting Point (° C.) 145-146 C-0007 Reflactive Index (n_(D) ²⁰) 1.529 C-0008 Melting Point (° C.) 167-169 C-0009 Reflactive Index (n_(D) ²⁰) 1.5245 C-0010 Melting Point (° C.) 173-174 C-0011 Melting Point (° C.) 117-120 C-0013 Reflactive Index (n_(D) ²⁰) 1.4918 C-0014 Reflactive Index (n_(D) ²⁰) 1.5275 C-0016 Melting Point (° C.) 149-150

TABLE 65 Physical Property Compound No. (¹H-NMR DATA, in CDCl₃/TMS δ (ppm)) A-0231 400 MHz 2.48(3H, s), 3.32(2H, q), 6.11(1H, d), 7.08 (1H, d), 7.43(1H, d) A-0234 400 MHz 3.37-3.47(1H, m), 3.70-3.81(1H, m), 6.16 (1H, d), 7.38(1H, d), 7.94(1H, d) A-0256 300 MHz 1.70-1.91(4H, m), 2.27-2.46(5H, m), 3.29 (2H, q), 4.03(2H, t), 6.96(1H, d), 7.13 (1H, d) A-0257 300 MHz 1.71-1.94(4H, m), 2.30-2.46(5H, m), 3.29- 3.50(2H, m), 4.12(2H, t), 6.99(1H, d), 7.54(1H, d) A-0259 300 MHz 2.37(3H, s), 3.30-3.51(2H, m), 5.30(1H, dd), 5.59(1H, dd), 6.19-6.51(1H, m), 7.11 (1H, d), 7.77(1H, d) A-0267 400 MHz 1.96-2.15(4H, m), 3.45(2H, q), 3.52(2H, t), 4.06(2H, t), 7.14(1H, s), 7.46(1H, s) A-0283 400 MHz 1.50-1.60(4H, m), 1.81-1.93(4H, m), 3.39- 3.49(4H, m), 4.02(2H, t), 7.13(1H, s), 7.45(1H, s) A-0284 300 MHz 1.53(4H, m), 1.70-2.03(4H, m), 2.17(3H, s), 2.38(3H, s), 3.26-3.43(4H, m), 3.94 (2H, t), 6.96(1H, s), 6.99(1H, s) A-0292 300 MHz 2.49(3H, s), 3.29(2H, q), 3.97(2H, t), 4.13(2H, t), 6.98(1H, d), 7.49(1H, d) A-0317 300 MHz 1.54-1.81(8H, m), 2.07-2.10(2H, m), 2.41 (3H, s), 3.30(2H, q), 3.94(2H, d), 6.96 (1H, d), 7.16(1H, d) A-0328 400 MHz 1.23-1.40(2H, m), 1.61-1.90(7H, m), 2.04- 2.16(2H, m), 2.41(3H, s), 3.29(2H, q), 4.05(2H, t), 6.97(1H, d), 7.15(1H, d) A-0329 400 MHz 1.23-1.51(2H, m), 1.60-1.88(7H, m), 2.03- 2.16(2H, m), 3.41(2H, q), 4.06(2H, t), 7.21(1H, d), 7.23(1H, d) A-0410 300 MHz 2.16-2.25(5H, m), 2.39(3H, s), 3.11(2H, t), 3.31(2H, q), 4.05(2H, t), 6.97(1H, s), 7.01(1H, s)

TABLE 66 Physical Property Compound No. (¹H-NMR DATA, in CDCl₃/TMS δ (ppm)) A-0411 300 MHz 2.22-2.31(8H, m), 3.12(2H, t), 3.27-3.50(2H, m), 4.16(2H, m), 7.03(1H, s), 7.38(1H, s) A-0412 300 MHz 2.21-2.29(2H, m), 3.15(2H, t), 3.45(2H, q), 4.11(2H, t), 7.15(1H, s), 7.47(1H, s) A-0413 400 MHz 2.28(2H, quint), 3.15(2H, t), 3.32-3.44(1H, m), 3.69-3.81(1H, m), 4.25(2H, t), 7.48(1H, s), 7.50(1H, s) A-0416 300 MHz 1.90-2.04(4H, m), 2.36(3H, s), 2.97(2H, t), 3.24-3.50(2H, m), 4.13(2H, t), 7.03(1H, d), 7.54(1H, d) A-0424 400 MHz 1.90-2.02(4H, m), 3.01(2H, t), 3.45(2H, q), 4.05(2H, t), 7.13(1H, s), 7.46(1H, s) A-0425 400 MHz 1.94-2.03(4H, m), 3.01(2H, t), 3.31-3.43 (1H, m), 3.68-3.81(1H, m), 4.17(2H, t), 7.18 (2H, s) A-0432 400 MHz 1.62(2H, m), 1.70-1.95(4H, m), 2.31(3H, s), 2.92(2H, t), 3.32-3.48(2H, m), 4.11(2H, t), 6.98(1H, d), 7.54(1H, d) A-0436 400 MHz 1.55-1.70(2H, m), 1.75-1.93(4H, m), 2.92 (2H, t), 3.51(2H, q), 4.10(2H, t), 7.25(1H, d), 7.41(1H, d) A-0440 300 MHz 1.54-1.67(2H, m), 1.70-1.95(4H, m), 2.39 (3H, s), 2.92(2H, t), 3.33(2H, q), 4.01(2H, t), 7.06(1H, s), 7.24(1H, s) A-0480 400 MHz 1.49-1.53(4H, m), 1.71-1.82(4H, m), 2.17 (3H, s), 2.38(3H, s), 2.90(2H, t), 3.30(2H, q), 3.94(2H, t), 6.96(1H, s), 6.70(1H, s) A-0511 300 MHz 1.40-1.56(6H, m), 1.66-1.83(4H, m), 2.17 (3H, s), 2.38(3H, s), 2.88(1H, t), 3.31(2H, q), 3.93(2H, t), 6.96(1H, s), 7.00(1H, s) A-0512 300 MHz 1.41-1.52(6H, m), 1.68-1.86(4H, m), 2.28 (3H , s), 2.33(3H, s), 2.89(2H, t), 3.26-3.50 (2H, m), 4.03(2H, t), 7.01(1H, s), 7.36(1H, s) A-0544 300 MHz 1.81-2.01(4H, m), 2.31(3H, s), 2.90(2H, t), 3.31-3.48(2H, m), 4.13(2H, t), 6.82(1H, t), 6.99(1H, d), 7.54(1H, d)

TABLE 67 Physical Property Compound No. (¹H-NMR DATA, in CDCl₃/TMS δ (ppm)) A-0554 400 MHz 1.57-1.63(2H, m), 1.75-1.89(4H, m), 2.31 (3H, s), 2.84(2H, t), 3.36-3.42(2H, m), 4.10 (2H, t), 6.81(1H, t), 7.00(1H, d), 7.54(1H, d) A-0557 400 MHz 1.57-1.63(2H, m), 1.72-1.84(4H, m), 2.38 (3H, s), 2.84(2H, t), 3.40(2H, q), 3.94(2H, t), 6.75(1H, dd), 6.81(1H, t), 7.00(1H, s), 7.11(1H, d) A-0570 400 MHz 1.49-1.56(4H, m), 1.70-1.81(4H, m), 2.41 (3H, s), 2.81(2H, t), 3.29(2H, q), 4.00(2H, t), 6.80(1H, t), 6.96(1H, d), 7.14(1H, d) A-0661 400 MHz 1.59-70(2H, m), 1.79-1.92(4H, m), 3.21 (2H, t), 3.41(2H, q), 4.04(2H, t), 7.21(1H, d), 7.25(2H, d) A-0664 300 MHz 2.17(3H, s), 2.34(2H, quint), 2.39(3H, s), 3.19(2H, t), 3.32(2H, q), 4.09(2H, t), 6.98 (1H, s), 7.01(1H, s) A-0678 400 MHz 1.50-1.62(4H, m), 1.83-1.92(4H, m), 2.96 (2H, t), 3.45(2H, q), 4.03(2H, t), 7.13(1H, s), 7.46(1H, s) A-0679 300 MHz 1.53-1.54(4H, m), 1.82-1.87(4H, m), 2.17 (3H, s), 2.38(3H, s), 2.96(2H, t), 3.31(2H, q), 3.94(2H, t), 6.96(1H, s), 6.70(1H, s) A-0681 300 MHz 1.40-1.56(6H, m), 1.75-1.88(4H, m), 2.17 (3H, s), 2.38(3H, s), 2.95(2H, t), 3.31(2H, q), 3.93(2H, t), 6.96(1H, s), 7.00(1H, s) A-0687 300 MHz 2.40(3H, s), 3.23(2H, q), 5.31(2H, s), 6.99 (1H, d), 7.12(1H, d), 7.46(1H, t), 7.57(1H, t), 7.63-7.80(2H, m) A-0745 300 MHz 2.42(3H, s) 3.24(2H, q) 5.14(2H, s), 7.00 (1H, d), 7.15(1H, d), 7.21-7.37(2H, m), 7.62(1H, dd) A-0747 300 MHz 2.41(3H, s), 3.21(2H, q), 5.17(2H, s), 7.00 (1H, d), 7.15(1H, d), 7.57(2H, d), 7.64(2H, d) A-0822 300 MHz 2.41(3H, s), 3.15(2H, t), 3.27(2H, q), 4.23 (2H, t), 6.96(1H, d), 7.11(1H, d), 7.11-7.19 (2H, m), 7.55(1H, t) A-0834 400 MHz 2.12(2H, quint), 2.41(3H, s), 2.82(2H, t), 3.27(2H, q), 4.01(2H, t), 6.96(1H, d), 7.11 (1H, d), 7.19-7.32(5H, m)

TABLE 68 Physical Property Compound No. (¹H-NMR DATA, in CDCl₃/TMS δ (ppm)) A-0970 300 MHz 1.10(9H, s), 2.16(2H, t), 2.41(3H, s), 3.29 (2H, q), 4.11-4.20(4H, m), 6.95(1H, d), 7.14 (1H, d), 7.32(1H, s) A-0971 400 MHz 1.09(9H, s), 2.18(2H, t), 2.31(3H, s), 3.30- 3.50(2H, m), 4.16-4.20(4H, m), 6.98(1H, d), 7.32(1H, s), 7.57(1H, d) A-0998 400 MHz 2.40(3H, s), 3.26(2H, q), 4.26(2H, t), 4.51 (2H, t), 6.98(1H, d), 7.25(1H, dd), 7.33-7.40 (1H, m), 7.47(1H, t), 7.55-7.65(2H, m), 7.65 (1H, d), 8.13(1H, s) A-1032 400 MHz 2.42(3H, s), 3.09(3H, s), 3.29(2H, q), 4.25- 4.35(2H, m), 4.56-4.61(2H, m), 6.99(1H, d), 7.18(1H, d) A-1044 400 MHz 2.10(2H, quint), 2.01(3H, s), 3.29(2H, q), 3.87(2H, t), 4.10(2H, t), 5.40(2H, bs), 6.96 (1H, d), 7.18(1H, d) A-1072 400 MHz 1.83-1.97(4H, m), 2.85(2H, t), 3.41(2H, q), 4.05(2H, t), 7.20(1H, d), 7.23(1H, d) A-1101 300 MHz 1.40(2H, bs), 1.59-1.70(2H, m), 1.79-1.89 (2H, m), 2.41(3H, s), 2.78(2H, t), 3.29(2H, q), 4.03(2H, t), 6.95(1H, d), 7.15(1H, s) A-1116 400 MHz 1.80-1.93(4H, m), 2.42(3H, s), 3.29(2H, q), 3.43-3.54(2H, m), 4.06(2H, t), 6.62(1H, bs), 6.98(1H, d), 7.15(1H, d) A-1149 400 MHz 1.78-1.94(4H, m), 2.41(3H, s), 2.97(3H, s), 3.24(2H, t), 3.30(2H, q), 4.05(2H, t), 4.44 (1H, bs), 6.97(1H, d), 7.15(1H, d) A-1156 300 MHz 1.80-1.99(4H, m), 3.36-3.47(4H, m), 4.07 (2H, t), 5.15(1H, m), 7.23(1H, d), 7.25(1H, d) A-1201 400 MHz 1.48-1.57(2H, m), 1.75-1.88(4H, m), 2.41 (3H, s), 3.29(2H, q), 3.82(2H, t), 3.92(3H, s), 4.11(2H, t), 6.96(1H, s), 7.14(1H, s)

TABLE 69 Physical Property Compound No. (¹H-NMR DATA, in CDCl₃/TMS δ (ppm)) B-0028 300 MHz 2.42(3H, s), 3.24(2H, q), 5.13(2H, s), 7.01 (1H, d), 7.15(1H, d), 7.30-7.38(2H, m), 8.60- 8.68(2H, m) B-0031 300 MHz 2.41(3H, s), 3.19-3.37(2H, m), 5.30(2H, s), 7.00(1H, d), 7.17(1H, d), 7.71(1H, d), 7.97 (1H, d), 8.86(1H, s) B-0057 300 MHz 2.15(2H, quint), 2.42(3H, s), 2.94(2H, t), 3.31(2H, q), 4.03(2H, t), 6.98(1H, d), 7.13 (1H, d), 7.62(1H, d), 7.72(1H, d), 8.60(1H, s) B-0060 300 MHz 2.32(2H, quint), 2.41(3H, s), 3.22(2H, t), 3.28(2H, q), 4.13(2H, t), 6.95(1H, d), 7.15 (1H, d), 7.88(1H, s), 8.70(1H, s) B-0063 300 MHz 2.44(3H, s), 3.29(2H, q), 5.33(2H, s), 7.04 (1H, d), 7.22(1H, d), 9.26(1H, s), 9.35(1H, s)

TABLE 70 Physical Property Compound No. (¹H-NMR DATA, in CDCl₃/TMS δ (ppm)) C-0005 400 MHz 2.36(3H, s), 3.38(2H, q), 5.61(1H, brs), 6.69(1H, dd), 6.93(1H, s), 7.03(1H, d) C-0006 400 MHz 2.28(3H, s), 3.37-3.56(2H, m), 6.96(1H, dd), 7.12(1H, d), 7.73(1H, d), 8.04(1H, bs) C-0015 300 MHz 3.30-3.44(1H, m), 3.66-3.80(1H, m), 7.40(1H, s), 7.61(1H, s) C-0017 300 MHz 2.20(3H, s), 2.36(3H, s), 3.32(2H, q), 4.59(1H, s), 6.93(1H, s), 6.98(1H, s) C-0018 300 MHz 2.25(6H, s), 3.35-3.53(2H, m), 6.98 (1H, s), 7.63(1H, s), 7.69(1H, s)

TABLE 71 Compound No. Specific Rotation (−)-A-0086 −104.4 (+)-A-0086 +103.6 (−)-A-0434 −120.3 (+)-A-0434 +119.3 (−)-A-0479 −120.6 (+)-A-0479 +115.2 (−)-A-0481  −93.2 (+)-A-0481  +96.5 (−)-A-0764  −86.4 (+)-A-0764  +88.5 (−)-A-0767 −117.0 (+)-A-0767 +122.8 (−)-A-1215  −99.2 (+)-A-1215  +98.1 (−)-A-1218 −120.4 (+)-A-1218 +121.6

Next, there are specifically explained examples of formulating the present pest control agent by using the present alkyl phenyl sulfide derivative produced as above or the agriculturally acceptable salt thereof. The kinds and proportions of compounds and additives used in each formulation are not restricted to those shown in the following Formulation Examples and may be varied in a wide range. In the following explanation, “parts (part)” refer (refers) to mass parts (mass part).

Formulation Example 1 Emulsifiable Concentrate

A compound described in Table 1 to Table 41 10 parts Cyclohexanone 30 parts Polyoxyethylene alkyl aryl ether 11 parts Calcium alkylbenzenesulfonate 4 parts Methylnaphthalene 45 parts

The above materials were dissolved homogeneously to obtain an emulsifiable concentrate.

Formulation Example 2 Wettable Powder

A compound described in Table 1 to Table 41 10 parts Sodium salt of naphthalenesulfonic acid- 0.5 part formalin condensate Polyoxyethylene alkyl aryl ether 0.5 part Diatomaceous earth 24 parts Clay 65 parts

The above materials were mixed and ground to obtain a wettable powder.

Formulation Example 3 Dust Formulation

A compound described in Table 1 to Table 41 2 parts Diatomaceous earth 5 parts Clay 93 parts

The above materials were mixed and ground to obtain a dust formulation.

Formulation Example 4 Granule

A compound described in Table 1 to table 41 5 parts Sodium salt of lauryl alcohol sulfate 2 parts Sodium ligninsulfonate 5 parts Carboxymethyl cellulose 2 parts Clay 86 parts

The above materials were mixed homogeneously and ground. Thereto was added 20 parts of water, followed by kneading. The kneaded material was passed through an extrusion-granulator to obtain granules of 14 to 32 meshes. The granules were dried to obtain a granule.

Formulation Example 5 Flowable Concentrate

A compound described in Table 1 to Table 41 20 parts Polyoxyethylene styrenated phenyl ether 4 parts sulfate Ethylene glycol 7 parts Silicone AF-118N (produced by Asahi 0.02 part Chemical Industry Co. , Ltd. ) Water 68.98 parts

The above materials were mixed for 30 minutes using a high-speed stirrer and then ground using a wet grinder to obtain a flowable concentrate.

The next, the effect of the present pest control agent is shown by Test Examples.

Test Example 1 Control Effect Test for Tetranychus urticae Koch (Two Spotted Spider Mite)

A wettable powder prepared based on Formulation Example 2 was diluted with water into an active ingredient concentration of 4 ppm. In the solution were immersed soybean seedlings which had been inoculated with 35 female adults of two spotted spider mite. The soybean seedlings were dried in the air and placed in a thermostat of 25° C. After 13 days, the number of living female adults was examined and the control value of the active ingredient was determined using the calculation formula of the following Mathematical Expression 1. This test was conducted with no replication.

Control value=100−[(number of living female adults after 13 days, in treated seedlings)/(number of living female adults after 13 days, in non-treated seedlings)]×100  [Mathematical Expression 1]

Tests similar to the above were conducted using, as comparative compounds, compound Nos. 22 and 23 described in JP-A-1975-29744, compound Nos. 3, 4, 5, 6 described in JP-A-1976-19121 and compound Nos. 18, 19 and 36 described in JP-A-1988-41451. The structures of these comparative compounds are as follows.

Compound Nos. of the compounds which gave, in the above test, a control value of 90 or above, are shown below. A-0013, A-0017, A-0018, A-0024, A-0047, A-0052, A-0055, A-0056, A-0075, A-0077, A-0078, A-0079, A-0085, A-0086, A-0088, A-0089, A-0090, A-0092, A-0094, A-0108, A-0113, A-0115, A-0116, A-0117, A-0120, A-0123, A-0125, A-0126, A-0130, A-0133, A-0141, A-0144, A-0145, A-0147, A-0157, A-0160, A-0164, A-0168, A-0170, A-0175, A-0181, A-0185, A-0204, A-0212, A-0216, A-0220, A-0222, A-0223, A-0224, A-0244, A-0257, A-0262, A-0271, A-0277, A-0316, A-0318, A-0319, A-0320, A-0321, A-0322, A-0324, A-0325, A-0326, A-0327, A-0328, A-0329, A-0330, A-0331, A-0338, A-0339, A-0340, A-0341, A-0343, A-0346, A-0347, A-0352, A-0353, A-0356, A-0359, A-0360, A-0363, A-0365, A-0368, A-0369, A-0379, A-0387, A-0388, A-0391, A-0392, A-0393, A-0394, A-0396, A-0406, A-0416, A-0418, A-0432, A-0434, A-0438, A-0439, A-0440, A-0441, A-0443, A-0444, A-0445, A-0446, A-0447, A-0448, A-0449, A-0471, A-0472, A-0473, A-0474, A-0475, A-0476, A-0477, A-0478, A-0479, A-0481, A-0482, A-0483, A-0484, A-0485, A-0487, A-0489, A-0495, A-0502, A-0503, A-0504, A-0505, A-0507, A-0508, A-0510, A-0524, A-0525, A-0526, A-0533, A-0536, A-0539, A-0543, A-0544, A-0553, A-0554, A-0555, A-0556, A-0557, A-0558, A-0559, A-0560, A-0561, A-0562, A-0563, A-0570, A-0571, A-0573, A-0574, A-0575, A-0576, A-0577, A-0578, A-0587, A-0588, A-0589, A-0590, A-0591, A-0592, A-0594, A-0599, A-0605, A-0606, A-0610, A-0611, A-0616, A-0617, A-0618, A-0622, A-0623, A-0625, A-0626, A-0631, A-0632, A-0638, A-0640, A-0642, A-0644, A-0665, A-0674, A-0683, A-0684, A-0686, A-0690, A-0692, A-0693, A-0694, A-0695, A-0697, A-0698, A-0703, A-0709, A-0710, A-0711, A-0712, A-0713, A-0716, A-0717, A-0724, A-0728, A-0734, A-0735, A-0736, A-0741, A-0743, A-0744, A-0745, A-0746, A-0748, A-0751, A-0752, A-0753, A-0754, A-0755, A-0757, A-0758, A-0761, A-0762, A-0763, A-0764, A-0765, A-0766, A-0767, A-0768, A-0769, A-0772, A-0773, A-0774, A-0775, A-0776, A-0778, A-0779, A-0780, A-0781, A-0782, A-0783, A-0784, A-0786, A-0787, A-0788, A-0789, A-0790, A-0791, A-0792, A-0793, A-0797, A-0798, A-0799, A-0800, A-0802, A-0805, A-0806, A-0807, A-0808, A-0809, A-0810, A-0813, A-0814, A-0816, A-0817, A-0818, A-0819, A-0820, A-0821, A-0822, A-0823, A-0824, A-0825, A-0826, A-0827, A-0838, A-0839, A-0844, A-0845, A-0853, A-0855, A-0856, A-0857, A-0860, A-0869, A-0870, A-0878, A-0880, A-0881, A-0885, A-0902, A-0913, A-0914, A-0915, A-0916, A-0917, A-0918, A-0921, A-0923, A-0924, A-0936, A-0940, A-0941, A-0942, A-0948, A-0956, A-0957, A-0969, A-0971, A-0973, A-0978, A-0979, A-0980, A-0982, A-0983, A-0984, A-0985, A-0988, A-0989, A-0990, A-0991, A-0992, A-1011, A-1032, A-1033, A-1052, A-1081, A-1087, A-1088, A-1107, A-1108, A-1112, A-1113, A-1119, A-1125, A-1126, A-1127, A-1128, A-1132, A-1136, A-1138, A-1140, A-1142, A-1149, A-1150, A-1151, A-1152, A-1154, A-1155, A-1156, A-1157, A-1158, A-1159, A-1164, A-1165, A-1166, A-1167, A-1175, A-1177, A-1178, A-1180, A-1181, A-1183, A-1185, A-1188, A-1190, A-1192, A-1195, A-1196, A-1200, A-1201, A-1207, A-1210, A-1211, B-0005, B-0006, B-0007, B-0008, B-0009, B-0010, B-0011, B-0017, B-0018, B-0019, B-0022, B-0023, B-0029, B-0055, B-0060, B-0063, B-0068, B-0070, B-0072, B-0073, B-0074, B-0075, B-0076, B-0078, B-0079, B-0080, B-0082, B-0084, B-0086, B-0088, B-0090, B-0092, B-0094, B-0096, B-0099, B-0102, B-0104, B-0106, B-0108

Any of comparative compounds 22 and 23 (described in JP-A-1975-29744), 3, 4, 5 and 6 (described in JP-A-1976-19121) and 18, 19 and 36 (described in JP-A-1988-41451) showed no activity at a concentration of 4 ppm.

Test Example 2 Insecticidal Activity Test for Nilaparvata lugens Stál (Brown Rice Planthopper)

A wettable powder prepared based on Formulation Example 2 was diluted with water into an active ingredient concentration of 100 ppm. In the solution was immersed sprouting unhulled rice. They were placed in a 60-ml plastic cup. Thereinto were released 10 3-instar larvae of brown rice planthopper. The cup was covered with a lid and placed in a thermostat of 25° C. After 6 days, the number of living insects was counted and the mortality of insect was determined from the calculation formula of the following Mathematical Expression 2. This test was conducted with no replication.

Mortality (%)=100−[(number of living insects after 6 days)/(number of tested insects)]×100  [Mathematical Expression 2]

As in the case of Test Example 1, tests similar to the above were conducted using, as comparative compounds, compound Nos. 22 and 23 described in JP-A-1975-29744, compound Nos. 4, 5, 6 described in JP-A-1976-19121 and compound Nos. 18, 19 and 36 described in JP-A-1988-41451.

Compound Nos. of the compounds which gave, in the above test, a mortality of 90% or above, are shown below. A-0001, A-0004, A-0005, A-0006, A-0007, A-0015, A-0018, A-0022, A-0023, A-0025, A-0032, A-0035, A-0037, A-0038, A-0039, A-0043, A-0044, A-0046, A-0047, A-0051, A-0052, A-0056, A-0070, A-0074, A-0075, A-0077, A-0078, A-0085, A-0086, A-0087, A-0088, A-0089, A-0090, A-0091, A-0092, A-0108, A-0122, A-0123, A-0125, A-0130, A-0133, A-0141, A-0144, A-0145, A-0147, A-0157, A-0159, A-0160, A-0163, A-0164, A-0167, A-0168, A-0169, A-0170, A-0172, A-0173, A-0175, A-0180, A-0181, A-0185, A-0186, A-0187, A-0188, A-0199, A-0200, A-0203, A-0205, A-0206, A-0208, A-0211, A-0212, A-0213, A-0214, A-0215, A-0216, A-0217, A-0218, A-0219, A-0220, A-0221, A-0222, A-0223, A-0224, A-0228, A-0229, A-0230, A-0243, A-0244, A-0253, A-0254, A-0256, A-0257, A-0259, A-0260, A-0262, A-0263, A-0266, A-0271, A-0277, A-0285, A-0307, A-0308, A-0311, A-0314, A-0317, A-0319, A-0324, A-0325, A-0328, A-0329, A-0338, A-0340, A-0341, A-0346, A-0360, A-0369, A-0379, A-0405, A-0406, A-0415, A-0416, A-0417, A-0418, A-0431, A-0432, A-0433, A-0434, A-0436, A-0437, A-0438, A-0439, A-0440, A-0446, A-0447, A-0448, A-0472, A-0473, A-0474, A-0475, A-0503, A-0504, A-0505, A-0535, A-0539, A-0543, A-0544, A-0553, A-0554, A-0556, A-0557, A-0570, A-0572, A-0574, A-0587, A-0610, A-0617, A-0625, A-0626, A-0631, A-0644, A-0683, A-0684, A-0703, A-0732, A-0734, A-0741, A-0743, A-0744, A-0745, A-0747, A-0751, A-0753, A-0755, A-0761, A-0763, A-0764, A-0765, A-0766, A-0772, A-0777, A-0778, A-0779, A-0780, A-0781, A-0786, A-0787, A-0788, A-0789, A-0797, A-0798, A-0809, A-0811, A-0813, A-0815, A-0821, A-0822, A-0823, A-0824, A-0825, A-0834, A-0838, A-0839, A-0844, A-0846, A-0847, A-0853, A-0855, A-0857, A-0877, A-0968, A-0969, A-0970, A-0971, A-0972, A-0973, A-0975, A-0976, A-0977, A-0978, A-0979, A-0981, A-0982, A-0983, A-0984, A-0985, A-0988, A-0991, A-0992, A-0998, A-1003, A-1004, A-1005, A-1006, A-1008, A-1009, A-1032, A-1033, A-1037, A-1044, A-1051, A-1087, A-1093, A-1094, A-1107, A-1125, A-1136, A-1140, A-1142, A-1158, A-1159, A-1177, A-1180, A-1185, A-1187, A-1188, A-1195, A-1210, A-1211, A-1212, A-1213, B-0003, B-0004, B-0005, B-0007, B-0012, B-0013, B-0022, B-0028, B-0029, B-0032, B-0033, B-0035, B-0051, B-0053, B-0055, B-0058, B-0059, B-0060, B-0063, B-0066, B-0086, B-0088, B-0093, B-0101, C-0001

Any of comparative compounds 22 and 23 (described in JP-A-1975-29744), 4, 5 and 6 (described in JP-A-1976-19121) and 18, 19 and 36 (described in JP-A-1988-41451) each showed no activity even at a concentration of 100 ppm. 

1-9. (canceled)
 10. An alkyl phenyl sulfide derivative represented by the general formula [I′] or an agriculturally acceptable salt thereof

wherein n is an integer of 0, 1 or 2, R^(1′) is a C₁-C₆ haloalkyl group (the group excludes 2-bromoethyl group), a C₂-C₈ alkenyl group (the group excludes allyl group), a C₂-C₈ haloalkenyl group, a C₂-C₆ alkynyl group, a C₂-C₆ haloalkynyl group, a branched C₄-C₆ alkyl group (the group excludes isobutyl group), a C₃-C₆ cycloalkyl C₁-C₆ alkyl group or a C₃-C₆ halocycloalkyl C₁-C₆ alkyl group, R^(2′) is a halogen atom, a C₁-C₆ alkyl group, a C₁-C₆ haloalkyl group, a C₃-C₆ cycloalkyl group, a C₃-C₆ halocycloalkyl group, a C₁-C₆ haloalkoxy group, a cyano group or a nitro group, R^(3′) is a hydrogen atom, a halogen atom, a C₁-C₆ alkyl group or a C₁-C₆ haloalkyl group.
 11. The alkyl phenyl sulfide derivative or an agriculturally acceptable salt thereof, according to claim 10, wherein R^(1′) in the general formula [I′] is a 2,2-difluoroethyl group, a 2,2,2-trifluoroethyl group, a 3,3,3-trifluoropropyl group, a pentafluoroethyl group, a 1,2,2,2-tetrafluoroethyl group, a 2-chloro-2,2-difluoroethyl group, a 2,2,3,3-tetrafluoropropyl group, a 2,2,3,3,3-pentafluoropropyl group, a 3,3-dichloroallyl group, a propargyl group, a cyclopropylmethyl group or a (2,2-difluorocyclopropyl)methyl group.
 12. The alkyl phenyl sulfide derivative or an agriculturally acceptable salt thereof, according to claim 10, wherein R^(2′) in the general formula [I′] is a halogen atom, a C₁-C₆ alkyl group, a C₁-C₆ haloalkyl group or a cyano group.
 13. The alkyl phenyl sulfide derivative or an agriculturally acceptable salt thereof, according to claim 10, wherein R^(3′) in the general formula [I′] is a hydrogen atom, a halogen atom or a C₁-C₆ alkyl group.
 14. The alkyl phenyl sulfide derivative or an agriculturally acceptable salt thereof, according to claim 11, wherein R^(2′) in the general formula [I′] is a halogen atom, a C₁-C₆ alkyl group, a C₁-C₆ haloalkyl group or a cyano group.
 15. The alkyl phenyl sulfide derivative or an agriculturally acceptable salt thereof, according to claim 11, wherein R^(3′) in the general formula [I′] is a hydrogen atom, a halogen atom or a C₁-C₆ alkyl group.
 16. An alkyl phenyl sulfide derivative or an agriculturally acceptable salt thereof, according to claim 12, wherein R^(3′) in the general formula [I′] is a hydrogen atom, a halogen atom or a C₁-C₆ alkyl group.
 17. A pest control agent which contains, as an active ingredient, an alkyl phenyl sulfide derivative or an agriculturally acceptable salt thereof, according to claim
 10. 18. A pest control agent which contains, as an active ingredient, an alkyl phenyl sulfide derivative or an agriculturally acceptable salt thereof, according to claim
 11. 19. A pest control agent comprising an alkyl phenyl sulfide derivative or an agriculturally acceptable salt thereof, according to claim 13, as an active ingredient; and at least one additive component. 